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Sample records for electrochemical surface derivation

  1. Electrochemical surface derivation of glassy carbon by the reduction of triaryl- and alkyldiphenylsulfonium salts

    DEFF Research Database (Denmark)

    Vase, K.H.; Holm, A.H.; Norrman, Kion

    2008-01-01

    The range of materials susceptible to electrochemically assisted grafting onto carbon materials has been expanded to include a new group of compounds. This new approach is based on the reduction of symmetrical or unsymmetrical triarylsulfonium salts and alkyldiphenylsulfonium salts. Our findings...

  2. Electrochemical nitridation of metal surfaces

    Science.gov (United States)

    Wang, Heli; Turner, John A.

    2015-06-30

    Electrochemical nitridation of metals and the produced metals are disclosed. An exemplary method of electrochemical nitridation of metals comprises providing an electrochemical solution at low temperature. The method also comprises providing a three-electrode potentiostat system. The method also comprises stabilizing the three-electrode potentiostat system at open circuit potential. The method also comprises applying a cathodic potential to a metal.

  3. Characterization of electrochemically modified polycrystalline platinum surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Krebs, Leonard C. [State Univ. of New York (SUNY), Stony Brook, NY (United States); Ishida, Takanobu [State Univ. of New York (SUNY), Stony Brook, NY (United States)

    1991-12-01

    The characterization of electrochemically modified polycrystalline platinum surfaces has been accomplished through the use of four major electrochemical techniques. These were chronoamperometry, chronopotentiommetry, cyclic voltammetry, and linear sweep voltammetry. A systematic study on the under-potential deposition of several transition metals has been performed. The most interesting of these were: Ag, Cu, Cd, and Pb. It was determined, by subjecting the platinum electrode surface to a single potential scan between -0.24 and +1.25 VSCE while stirring the solution, that the electrocatalytic activity would be regenerated. As a consequence of this study, a much simpler method for producing ultra high purity water from acidic permanganate has been developed. This method results in water that surpasses the water produced by pyrocatalytic distillation. It has also been seen that the wettability of polycrystalline platinum surfaces is greatly dependent on the quantity of oxide present. Oxide-free platinum is hydrophobic and gives a contact angle in the range of 55 to 62 degrees. We have also modified polycrystalline platinum surface with the electrically conducting polymer poly-ρ-phenylene. This polymer is very stable in dilute sulfuric acid solutions, even under applied oxidative potentials. It is also highly resistant to electrochemical hydrogenation. The wettability of the polymer modified platinum surface is severely dependent on the choice of supporting electrolyte chosen for the electrochemical polymerization. Tetraethylammonium tetrafluoroborate produces a film that is as hydrophobic as Teflon, whereas tetraethylammonium perchlorate produces a film that is more hydrophilic than oxide-free platinum.

  4. Characterization of electrochemically modified polycrystalline platinum surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Krebs, L.C.; Ishida, Takanobu.

    1991-12-01

    The characterization of electrochemically modified polycrystalline platinum surfaces has been accomplished through the use of four major electrochemical techniques. These were chronoamperometry, chronopotentiommetry, cyclic voltammetry, and linear sweep voltammetry. A systematic study on the under-potential deposition of several transition metals has been performed. The most interesting of these were: Ag, Cu, Cd, and Pb. It was determined, by subjecting the platinum electrode surface to a single potential scan between {minus}0.24 and +1.25 V{sub SCE} while stirring the solution, that the electrocatalytic activity would be regenerated. As a consequence of this study, a much simpler method for producing ultra high purity water from acidic permanganate has been developed. This method results in water that surpasses the water produced by pyrocatalytic distillation. It has also been seen that the wettability of polycrystalline platinum surfaces is greatly dependent on the quantity of oxide present. Oxide-free platinum is hydrophobic and gives a contact angle in the range of 55 to 62 degrees. We have also modified polycrystalline platinum surface with the electrically conducting polymer poly-{rho}-phenylene. This polymer is very stable in dilute sulfuric acid solutions, even under applied oxidative potentials. It is also highly resistant to electrochemical hydrogenation. The wettability of the polymer modified platinum surface is severely dependent on the choice of supporting electrolyte chosen for the electrochemical polymerization. Tetraethylammonium tetrafluoroborate produces a film that is as hydrophobic as Teflon, whereas tetraethylammonium perchlorate produces a film that is more hydrophilic than oxide-free platinum.

  5. Regioselective Green Electrochemical Approach to the Synthesis of Nitroacetaminophen Derivatives.

    Science.gov (United States)

    Salahifar, Eslam; Nematollahi, Davood; Bayat, Mehdi; Mahyari, Amir; Amiri Rudbari, Hadi

    2015-10-02

    A regioselective green synthesis of nitroacetaminophen derivatives was carried out by electrochemical oxidation of acetaminophen, N-(2-hydroxyphenyl)acetamide, and 1-(4-(4-hydroxyphenyl)piperazin-1-yl)ethanone in the presence of nitrite ion as a nucleophile. The present work has led to the development of a reagentless green and facile electrochemical method for the synthesis of some nitroacetaminophen derivatives.

  6. Electrochemical, surface analytical and quantum chemical studies ...

    Indian Academy of Sciences (India)

    Home; Journals; Bulletin of Materials Science; Volume 34; Issue 6. Electrochemical, surface analytical and quantum chemical studies on Schiff bases of 4-amino-4H-1, 2, 4-triazole-3,5-dimethanol (ATD) in corrosion protection of aluminium in 1N HNO3. Sam John K Mohammad Ali Abraham Joseph. Volume 34 Issue 6 ...

  7. Electrochemical components employing polysiloxane-derived binders

    Science.gov (United States)

    Delnick, Frank M.

    2013-06-11

    A processed polysiloxane resin binder for use in electrochemical components and the method for fabricating components with the binder. The binder comprises processed polysiloxane resin that is partially oxidized and retains some of its methyl groups following partial oxidation. The binder is suitable for use in electrodes of various types, separators in electrochemical devices, primary lithium batteries, electrolytic capacitors, electrochemical capacitors, fuel cells and sensors.

  8. Biomass derived porous nitrogen doped carbon for electrochemical devices

    Directory of Open Access Journals (Sweden)

    Litao Yan

    2017-04-01

    Full Text Available Biomass derived porous nanostructured nitrogen doped carbon (PNC has been extensively investigated as the electrode material for electrochemical catalytic reactions and rechargeable batteries. Biomass with and without containing nitrogen could be designed and optimized to prepare PNC via hydrothermal carbonization, pyrolysis, and other methods. The presence of nitrogen in carbon can provide more active sites for ion absorption, improve the electronic conductivity, increase the bonding between carbon and sulfur, and enhance the electrochemical catalytic reaction. The synthetic methods of natural biomass derived PNC, heteroatomic co- or tri-doping into biomass derived carbon and the application of biomass derived PNC in rechargeable Li/Na batteries, high energy density Li–S batteries, supercapacitors, metal-air batteries and electrochemical catalytic reaction (oxygen reduction and evolution reactions, hydrogen evolution reaction are summarized and discussed in this review. Biomass derived PNCs deliver high performance electrochemical storage properties for rechargeable batteries/supercapacitors and superior electrochemical catalytic performance toward hydrogen evolution, oxygen reduction and evolution, as promising electrodes for electrochemical devices including battery technologies, fuel cell and electrolyzer. Keywords: Biomass, Nitrogen doped carbon, Batteries, Fuel cell, Electrolyzer

  9. Surface electrochemical control for fine coal and pyrite separation

    Energy Technology Data Exchange (ETDEWEB)

    Hu, Weibai; Huang, Qinping; Li, Jun; Riley, A.; Turcotte, S.B.; Benner, R.E.; Zhu, Ximeng; Bodily, D.M.; Liang, Jun; Zhong, Tinghe; Wadsworth, M.E.

    1991-01-01

    The ongoing work includes the characterization of coal pyrites, the floatability evaluation of three typical US coal samples, the flotation behavior of coal pyrites, the electrochemical measurement of the surface properties of coal pyrites, and the characterization of species produced at pyrite surfaces. This report covers a Raman spectroscopy of species produced electrochemically on pyrite surfaces.

  10. Concatenation of electrochemical grafting with chemical or electrochemical modification for preparing electrodes with specific surface functionality

    Energy Technology Data Exchange (ETDEWEB)

    Verma, Pallavi; Maire, Pascal [Paul Scherrer Institut, Electrochemistry Laboratory, Section Electrochemical Energy Storage, CH-5232 Villigen PSI (Switzerland); Novak, Petr, E-mail: petr.novak@psi.c [Paul Scherrer Institut, Electrochemistry Laboratory, Section Electrochemical Energy Storage, CH-5232 Villigen PSI (Switzerland)

    2011-04-01

    Surface modified electrodes are used in electro-analysis, electro-catalysis, sensors, biomedical applications, etc. and could also be used in batteries. The properties of modified electrodes are determined by the surface functionality. Therefore, the steps involved in the surface modification of the electrodes to obtain specific functionality are of prime importance. We illustrate here bridging of two routes of surface modifications namely electrochemical grafting, and chemical or electrochemical reduction. First, by electrochemical grafting an organic moiety is covalently immobilized on the surface. Then, either by chemical or by electrochemical route the terminal functional group of the grafted moiety is transformed. Using the former route we prepared lithium alkyl carbonate (-O(CH{sub 2}){sub 3}OCO{sub 2}Li) modified carbon with potential applications in batteries, and employing the latter we prepared phenyl hydroxyl amine (-C{sub 6}H{sub 4}NHOH) modified carbon which may find application in biosensors. Benzyl alcohol (-C{sub 6}H{sub 4}CH{sub 2}OH) modified carbon was prepared by both chemical as well as electrochemical route. We report combinations of conjugating the two steps of surface modifications and show how the optimal route of terminal functional group modification depends on the chemical nature of the moiety attached to the surface in the electrochemical grafting step.

  11. Electrochemical and optical sugar sensors based on phenylboronic acid and its derivatives

    Energy Technology Data Exchange (ETDEWEB)

    Egawa, Yuya; Seki, Toshinobu [Faculty of Pharmaceutical Sciences, Josai University, Keyakidai, Sakado, Saitama 350-0295 (Japan); Takahashi, Shigehiro [Graduate School of Pharmaceutical Sciecnes, Tohoku University, Aramaki, Aoba-ku, Sendai 980-8578 (Japan); Anzai, Jun-ichi, E-mail: junanzai@mail.pharm.tohoku.ac.jp [Graduate School of Pharmaceutical Sciecnes, Tohoku University, Aramaki, Aoba-ku, Sendai 980-8578 (Japan)

    2011-10-10

    Recent progress in electrochemical and optical sugar sensors based on phenylboronic acid (PBA) and its derivatives as recognition components is reviewed. PBAs are known to bind diol compounds including sugars to form cyclic boronate esters that are negatively charged as a result of the addition of OH{sup -} ions from solution. Based on the formation of PBA charged species, sugars and their derivatives can be detected by means of electrochemical and optical techniques. For the development of PBA-based electrochemical sensing systems or sensors, PBA is modified with a redox-active marker, because PBA itself is electrochemically inactive, and ferrocene derivatives are often employed for this purpose. Ferrocene-modified PBAs have been used as redox-active additives in solution for the electrochemical detection of sugars and derivatives. PBA-modified electrodes have also been constructed as reagentless electrochemical sensors, where PBAs are immobilized on the surface of metal and carbon electrodes through mainly two routes: as a self-assembled monolayer film and as a polymer thin film. PBA-modified electrodes can be successfully used to detect sugars and derivatives through potentiometric and voltammetric responses. In addition, PBA-modified electrodes can be used for the immobilization of glycoenzymes on an electrode surface by the formation of boronate esters with carbohydrate chains in the glycoenzymes, thus resulting in enzyme biosensors. For the development of PBA-based optical sensors, a variety of chromophores and fluorophores have been coupled with PBA. Azobenzene dyes have been most frequently used for the preparation of colorimetric sugar sensors, in which the absorption wavelength and intensity of the dye are dependent on the type and concentration of added sugars. The sensitivity of the sensors is significantly improved based on multi-component systems in which alizalin red S, pyrocatechol violet, starch-iodine complex, and cyclodextrin are employed as

  12. Surface electrochemical control for the fine coal and pyrite separation

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Wanxiong; Hu, Weibai; Wann, Jyi-Perng; Zhu, Ximeng; Wadsworth, M.E.; Bodily, D.M.

    1989-01-01

    Ongoing work includes the characterization of coal pyrites, the floatability evaluation of typical US coal samples, the flotation behavior of coal pyrites, the electrochemical measurement of the surface properties of coal pyrites, and the characterization of species produced at pyrite surfaces.

  13. In Situ Investigation of Electrochemically Mediated Surface-Initiated Atom Transfer Radical Polymerization by Electrochemical Surface Plasmon Resonance.

    Science.gov (United States)

    Chen, Daqun; Hu, Weihua

    2017-04-18

    Electrochemically mediated atom transfer radical polymerization (eATRP) initiates/controls the controlled/living ATRP chain propagation process by electrochemically generating (regenerating) the activator (lower-oxidation-state metal complex) from deactivator (higher-oxidation-state metal complex). Despite successful demonstrations in both of the homogeneous polymerization and heterogeneous systems (namely, surface-initiated ATRP, SI-ATRP), the eATRP process itself has never been in situ investigated, and important information regarding this process remains unrevealed. In this work, we report the first investigation of the electrochemically mediated SI-ATRP (eSI-ATRP) by rationally combining the electrochemical technique with real-time surface plasmon resonance (SPR). In the experiment, the potential of a SPR gold chip modified by the self-assembled monolayer of the ATRP initiator was controlled to electrochemically reduce the deactivator to activator to initiate the SI-ATRP, and the whole process was simultaneously monitored by SPR with a high time resolution of 0.1 s. It is found that it is feasible to electrochemically trigger/control the SI-ATRP and the polymerization rate is correlated to the potential applied to the gold chip. This work reveals important kinetic information for eSI-ATRP and offers a powerful platform for in situ investigation of such complicated processes.

  14. An electrochemical study of two self-dopable water-soluble aniline derivatives: electrochemical deposition of copolymers.

    Science.gov (United States)

    Vacareanu, Loredana; Catargiu, Ana-Maria; Grigoras, Mircea

    2012-01-01

    An electrochemical study of two water-soluble aniline derivatives, N-(3-sulfopropyl) aniline (AnPS) and N-(3-sulfopropyl) p-aminodiphenylamine (DAnPS), in aqueous acidic electrolytic solutions containing different kinds of doping anions (Cl (-), SO(4) (2-), and ClO(4) (-)) was carried out. At sufficiently high anodic potential, the sulfonated aniline derivatives undergo oxidation processes yielding cation-radical and dimer intermediates, but no polymer deposition was observed on the working electrode surface. Experimental results showed that both aniline derivatives are electroactive compounds exhibiting redox behaviour in the range of potential of -0.2 V-1.6 V. Due to the self-doping effect induced by sulfonic groups, AnPS and DAnPS compounds have good electroactivity even in neat water solution. By adding a small amount of aniline into electrolytic system, thin layers of copolymers were deposited on the working electrode surface. The copolymer layers formed on the electrodes show a highly orientational and positional order, confirmed by AFM and XRD spectroscopic techniques. During the anodic oxidation processes some distinct colour changes were observed.

  15. An Electrochemical Study of Two Self-Dopable Water-Soluble Aniline Derivatives: Electrochemical Deposition of Copolymers

    Directory of Open Access Journals (Sweden)

    Loredana Vacareanu

    2012-01-01

    Full Text Available An electrochemical study of two water-soluble aniline derivatives, N-(3-sulfopropyl aniline (AnPS and N-(3-sulfopropyl p-aminodiphenylamine (DAnPS, in aqueous acidic electrolytic solutions containing different kinds of doping anions (Cl −, SO4 2−, and ClO4 − was carried out. At sufficiently high anodic potential, the sulfonated aniline derivatives undergo oxidation processes yielding cation-radical and dimer intermediates, but no polymer deposition was observed on the working electrode surface. Experimental results showed that both aniline derivatives are electroactive compounds exhibiting redox behaviour in the range of potential of −0.2 V–1.6 V. Due to the self-doping effect induced by sulfonic groups, AnPS and DAnPS compounds have good electroactivity even in neat water solution. By adding a small amount of aniline into electrolytic system, thin layers of copolymers were deposited on the working electrode surface. The copolymer layers formed on the electrodes show a highly orientational and positional order, confirmed by AFM and XRD spectroscopic techniques. During the anodic oxidation processes some distinct colour changes were observed.

  16. Synthesis and electrochemical study of some novel alkynylferrocene derivatives

    Directory of Open Access Journals (Sweden)

    Rahman Hosseinzadeh

    2014-01-01

    Full Text Available Ferrocene and their derivatives are well-known redox active materials and were extensively used by construction of modified electrodes for the design of electrochemical sensors and biosensors. Substituent derivatization of ferrocene offers the prospect of controlling ferrocene moiety properties such as solubility, stability, reversibility of oxidation wave (important for their role as an electron transfer mediator and oxidation potential, which is critical in the electrochemical determination of biological compounds. A new series of rigid alkynylferrocene including of 2-ferrocenylethynyl fluoren (3a, 2-ferrocenylethynyl fluoren-9-one (3b, 4-ferrocenylethynyl aniline (3c and 3-ferrocenylethynyl-1-trifluoromethyl benzene (3d have been prepared in good yields by Sonogashira coupling reaction. All products were characterized by 1H and 13C NMR, FT-IR, and elemental analysis. The redox chemistry of these compounds has been investigated by cyclic voltammetry. The half-wave potential of the terminal ferrocenyl moieties increases progressively in the order of 3c<3a<3b<3d, which is consistent with the electron density on the ferrocenyl unit.

  17. Electrochemical Biosensors Based on Ferroceneboronic Acid and Its Derivatives: A Review

    Directory of Open Access Journals (Sweden)

    Baozhen Wang

    2014-07-01

    Full Text Available We review recent progress in the development of electrochemical biosensors based on ferroceneboronic acid (FcBA and ferrocene (Fc-modified boronic acids. These compounds can be used to construct electrochemical biosensors because they consist of a binding site (i.e., a boronic acid moiety and an electrochemically active part (i.e., an Fc residue. By taking advantage of the unique properties of FcBA and its derivatives, electrochemical sensors sensitive to sugars, glycated hemoglobin (HbA1c, fluoride (F− ions, and so forth have been widely studied. FcBA-based sugar sensors rely on the selective binding of FcBA to 1,2- or 1,3-diol residues of sugars through the formation of cyclic boronate ester bonds. The redox properties of FcBA-sugar adduct differ from those of free FcBA, which forms the basis of the electrochemical determination of sugars. Thus, non-enzymatic glucose sensors are now being actively studied using FcBA and Fc-modified boronic acids as redox markers. Using a similar principle, HbA1c can be detected by FcBA-based electrochemical systems because it contains hydrocarbon chains on the polypeptide chain. HbA1c sensors are useful for monitoring blood glucose levels over the preceding 8–12 weeks. In addition, FcBA and Fc-modified boronic acids have been used for the detection of F− ions due to the selective binding of boronic acid to F− ions. F−-ion sensors may be useful alternatives to conventional ion-selective electrodes sensitive to F− ion. Furthermore, FcBA derivatives have been studied to construct lectin; steroids; nucleotides; salicylic acid; and bacteria sensors. One of the limitations of FcBA-based sensors comes from the fact that FcBA derivatives are added in sample solutions as reagents. FcBA derivatives should be immobilized on the surface of electrodes for developing reagentless sensors.

  18. Immobilization of carbon nanotubes and metallophthalocyanines on conductive surfaces by electrochemical means for electroanalytical purposes

    Energy Technology Data Exchange (ETDEWEB)

    Porras Gutierrez, A.; Gutierrez Granados, S. [Centre national de la recherche scientifique, Paris (France). Unite de Pharmacologie Chimique et Genetique; Guanajuato Univ. Guanajuato (Mexico). Inst. de Investigaciones Cientificas; Richard, C.; Griveau, S.; Bedioui, F. [Centre national de la recherche scientifique, Paris (France). Unite de Pharmacologie Chimique et Genetique; Zagal, J.H. [Santiago Univ. de Chile, Santiago (Chile)

    2008-07-01

    Carbon nanotubes (CNT) have been touted as viable candidates for the design of new electrode materials because of their high conductivity and high specific surface area. This study explored the use of electrochemical methods to immobilize single walled carbon nanotubes (SWCNT) on glassy carbon (GC) in a stable and controlled fashion. Two electrochemical routes were investigated to get the stable immobilization of nanotubes, notably (1) electropolymerization of conducting polymers in presence of SWCNT, and (2) the electrochemical grafting of diazonium salts in presence of SWCNT. The objective was to obtain chemically and mechanically stable composite GC/SWCNT electrodes. The electrochemical performances and reactivity of the electrodes were analyzed by voltammetry and by scanning electrochemical microscopy. The optimized immobilization methods were then applied to the conception of electrocatalysts hybrids, by co-immobilization of nanotubes with well-known redox catalyst metallocomplexes for activation of the electro-oxidation of biologically relevant thiol. The study showed that the nanocomposite material based on the combined use of metallophthalocynines, functionalized SWCNTs and electropolymerizable matrices enables the assembly of highly stable electrodes with better electrocatalytic oxidation of thiols. This fast procedure to modify glassy carbon (GC) electrode using commercially available cobalt phthalocyanine (CoPc) and tetrasulfonated nickel phthalocyanine (NiTSPc), oxidized single walled carbon nanotubes SWCNT and electropolymerized polypyrrole or diazonium derivatives. It was concluded that the electrodes are highly stable and the tailored hybrid surfaces improves electron transfer. 4 refs.

  19. Electrochemically Inducible Surfaces for Patterning Two Distinct Molecules

    Energy Technology Data Exchange (ETDEWEB)

    Choi, Inseong; Yeo, Woon-Seok [Konkuk University,Seoul (Korea, Republic of)

    2016-04-15

    Herein, we report on a new multicomponent patterning method based on electrochemically inducible self-assembled monolayers on gold. Two different masked functional groups on monolayers are activated to give amine and acetylene moieties through electrochemical activations at negative potential and positive potential, respectively. The resulting amine and acetylene groups are further used as chemical handles for incorporation of ligand molecules via well-known chemoselective conjugation reactions such as amine-specific conjugation chemistry and click reaction. The chemical conversions of masked functional groups to amine and acetylene groups were characterized by cyclic voltammetry. We demonstrated the orthogonal immobilization of two fluorescent dyes on the patterned surface along the patterned features. Our strategy can provide a useful platform technology for the preparation of multicomponent ligand-patterned substrates with various advantages such as chemical flexibility, mild reaction conditions, and high yields of two orthogonal chemical reactions of amine-specific conjugation and click reaction.

  20. Derived limits for surface contamination

    CERN Document Server

    Wrixon, A D; Linsley, G S; White, D F

    1979-01-01

    Derived limits (DLs) for surface contamination were first established for use in the nuclear energy industry where a wide variety of radionuclides is encountered. They were later used in factories, hospitals, and universities, where the radionuclides used are normally fewer in number, either known or readily identifiable, and often of low toxicity. In these situations the current limits are frequently over-restrictive. This report describes a reassessment of the values in the light of more recent information on the possible pathways of exposure and the dose equivalent limits given in ICRP Publication 26. The reassessment is prompted also by the introduction of SI units. The results of the reassessment are used to produce a classification of DLs for all radionuclides for active and inactive area surfaces and for skin.

  1. Three-dimensional polypyrrole-derived carbon nanotube framework for dye adsorption and electrochemical supercapacitor

    Science.gov (United States)

    Xin, Shengchang; Yang, Na; Gao, Fei; Zhao, Jing; Li, Liang; Teng, Chao

    2017-08-01

    Three-dimensional carbon nanotube frameworks have been prepared via pyrolysis of polypyrrole nanotube aerogels that are synthesized by the simultaneous self-degraded template synthesis and hydrogel assembly followed by freeze-drying. The microstructure and composition of the materials are investigated by thermal gravimetric analysis, Raman spectrum, X-ray photoelectron spectroscopy, transmission electron microscopy, and specific surface analyzer. The results confirm the formation of three-dimensional carbon nanotube frameworks with low density, high mechanical properties, and high specific surface area. Compared with PPy aerogel precursor, the as-prepared three-dimensional carbon nanotube frameworks exhibit outstanding adsorption capacity towards organic dyes. Moreover, electrochemical tests show that the products possess high specific capacitance, good rate capability and excellent cycling performance with no capacitance loss over 1000 cycles. These characteristics collectively indicate the potential of three-dimensional polypyrrole-derived carbon nanotube framework as a promising macroscopic device for the applications in environmental and energy storages.

  2. Recent progress in electrochemical biosensors based on phenylboronic acid and derivatives.

    Science.gov (United States)

    Anzai, Jun-Ichi

    2016-10-01

    This review provides an overview of recent progress made in the development of electrochemical biosensors based on phenylboronic acid (PBA) and its derivatives. PBAs are known to selectively bind 1,2- and 1,3-diols to form negatively charged boronate esters in neutral aqueous media and have been used to construct electrochemical glucose sensors because of this selective binding. PBA-modified metal and carbon electrodes have been widely studied as voltammetric and potentiometric glucose sensors. In some cases, ferroceneboronic acid or ferrocene-modified phenylboronic acids are used as sugar-selective redox compounds. Another option for sensors using PBA-modified electrodes is potentiometric detection, in which the changes in surface potential of the electrodes are detected as an output signal. An ion-sensitive field effect transistor (FET) has been used as a signal transducer in potentiometric sensors. Glycoproteins, such as glycated hemoglobin (HbA1c), avidin, and serum albumin can also be detected by PBA-modified electrodes because they contain hydrocarbon chains on the surface. HbA1c sensors are promising alternatives to enzyme-based glucose sensors for monitoring blood glucose levels over the preceding 2-3months. In addition, PBA-modified electrodes can be used to detect a variety of compounds including hydroxy acids and fluoride (F(-)) ions. PBA-based F(-) ion sensors may be useful if reagentless sensors can be developed. Copyright © 2016 Elsevier B.V. All rights reserved.

  3. New insights into the electrochemical behavior of acid orange 7: Convergent paired electrochemical synthesis of new aminonaphthol derivatives.

    Science.gov (United States)

    Momeni, Shima; Nematollahi, Davood

    2017-02-06

    Electrochemical behavior of acid orange 7 has been exhaustively studied in aqueous solutions with different pH values, using cyclic voltammetry and constant current coulometry. This study has provided new insights into the mechanistic details, pH dependence and intermediate structure of both electrochemical oxidation and reduction of acid orange 7. Surprisingly, the results indicate that a same redox couple (1-iminonaphthalen-2(1H)-one/1-aminonaphthalen-2-ol) is formed from both oxidation and reduction of acid orange 7. Also, an additional purpose of this work is electrochemical synthesis of three new derivatives of 1-amino-4-(phenylsulfonyl)naphthalen-2-ol (3a-3c) under constant current electrolysis via electrochemical oxidation (and reduction) of acid orange 7 in the presence of arylsulfinic acids as nucleophiles. The results indicate that the electrogenerated 1-iminonaphthalen-2(1 H)-one participates in Michael addition reaction with arylsulfinic acids to form the 1-amino-3-(phenylsulfonyl)naphthalen-2-ol derivatives. The synthesis was carried out in an undivided cell equipped with carbon rods as an anode and cathode.

  4. Optically Designed Anodised Aluminium Surfaces: Microstructural and Electrochemical Aspects

    DEFF Research Database (Denmark)

    Gudla, Visweswara Chakravarthy

    Emission Spectroscopy, and Scanning Kelvin Probe Force Microscopy. Optical characterization was performed using integrating sphere measurements. Combining the results and understanding obtained from anodising of magnetron sputtered coatings, Al-TiO2 surface composites and their electrochemical behaviour...... particles. Theoretical modelling and physical modelling of the anodised layer with TiO2 particles were simulated using Polyurthenane-TiO2 coatings and investigating the optical appearance. The conventional DC anodising and high frequency pulse and pulse reverse pulse anodising were employed to generate...... bright-anodised surfaces. Effect of pulse frequency, anodic and cathodic cycle potential values was systematically investigated. Characterization of surfaces and substrates was performed using Scanning and Transmission Electron Microscopy, Grazing-Incidence X-ray Diffraction, Glow Discharge Optical...

  5. Electrochemical Study of Diphenyl Ether Derivatives Used as Herbicides

    Directory of Open Access Journals (Sweden)

    Amira Zaouak

    2011-01-01

    Full Text Available The electrochemical behaviour of five nitro diphenyl ethers used as herbicides is investigated in acetonitrile. A detailed study by cyclic voltammetry and exhaustive electrolysis is carried out for the anodic oxidation of 2-Chloro-6-nitro-3-phenoxyaniline (aclonifen and shows that the major oxidation product is a dimeric compound. A mechanistic scheme involving a coupling process is postulated for the electrochemical oxidation of this compound. Furthermore, the use of differential pulse voltammetry on a glassy carbon electrode permits the selective determination of aclonifen. The limit of detection is 0.6 μg/mL.

  6. Electrochemical characterization of organosilane-functionalized nanostructured ITO surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Pruna, R., E-mail: rpruna@el.ub.edu; Palacio, F.; López, M. [SIC, Departament d' Enginyeries: Electrònica, Universitat de Barcelona, C/ Martí i Franquès 1, E-08028 Barcelona (Spain); Pérez, J. [Nanobioengineering Group, Institute for Bioengineering of Catalonia (IBEC), Baldiri Reixac 15-21, E-08028 Barcelona (Spain); Mir, M. [Nanobioengineering Group, Institute for Bioengineering of Catalonia (IBEC), Baldiri Reixac 15-21, E-08028 Barcelona (Spain); Centro de Investigación Biomédica en Red en Bioingeniería, Biomateriales y Nanomedicina (CIBER-BBN), Monforte de Lemos 3-5 Pabellón 11, E-28029 Madrid (Spain); Blázquez, O.; Hernández, S.; Garrido, B. [MIND-IN" 2UB, Departament d' Enginyeries: Electrònica, Universitat de Barcelona, C/ Martí i Franquès 1, E-08028 Barcelona (Spain)

    2016-08-08

    The electroactivity of nanostructured indium tin oxide (ITO) has been investigated for its further use in applications such as sensing biological compounds by the analysis of redox active molecules. ITO films were fabricated by using electron beam evaporation at different substrate temperatures and subsequently annealed for promoting their crystallization. The morphology of the deposited material was monitored by scanning electron microscopy, confirming the deposition of either thin films or nanowires, depending on the substrate temperature. Electrochemical surface characterization revealed a 45 % increase in the electroactive surface area of nanostructured ITO with respect to thin films, one third lower than the geometrical surface area variation determined by atomic force microscopy. ITO surfaces were functionalized with a model organic molecule known as 6-(ferrocenyl)hexanethiol. The chemical attachment was done by means of a glycidoxy compound containing a reactive epoxy group, the so-called 3-glycidoxypropyltrimethoxy-silane. ITO functionalization was useful for determining the benefits of nanostructuration on the surface coverage of active molecules. Compared to ITO thin films, an increase in the total peak height of 140 % was observed for as-deposited nanostructured electrodes, whereas the same measurement for annealed electrodes resulted in an increase of more than 400 %. These preliminary results demonstrate the ability of nanostructured ITO to increase the surface-to-volume ratio, conductivity and surface area functionalization, features that highly benefit the performance of biosensors.

  7. Surface effects and electrochemical cell capacitance in desorption electrospray ionization.

    Science.gov (United States)

    Volný, Michael; Venter, Andre; Smith, Scott A; Pazzi, Marco; Cooks, R Graham

    2008-04-01

    Time resolved measurements show that during a desorption electrospray ionization (DESI) experiment, the current initially rises sharply, followed by an exponential decrease to a relatively steady current. When the high voltage on the spray emitter is switched off, the current drops to negative values, suggesting that the direction of current flow in the equivalent DESI circuit is reversed. These data demonstrate that the DESI source behaves as a dc capacitor and that the addition of a surface between the sprayer and the counter electrode in DESI introduces a new electrically active element into the system. The charging and discharging behavior was observed using different surfaces and it could be seen both by making current measurements on a plate at the entrance to the mass spectrometer as well as by measuring ion current in the linear ion trap within the vacuum system of the mass spectrometer. The magnitude of the steady state current obtained without analyte present on the surface is different for different surface materials, and different capacitor time constants of the equivalent RC circuits were calculated for different DESI surfaces. The PTFE surface has by far the greatest time constant and is also able to produce the highest DESI currents. Surface properties play a crucial role in charge transfer during DESI in addition to the effects of the chemical properties of the analyte. It is suggested that surface energy (wettability) is an important factor controlling droplet behavior on the surface. The experimental data are correlated with critical surface tension values of different materials. It is proposed, based on the results presented, that super-hydrophobic materials with extremely high contact angles have the potential to be excellent DESI substrates. It is also demonstrated, using the example of the neurotransmitter dopamine, that the surface charge that develops during a DESI-MS experiment can cause electrochemical oxidation of the analyte.

  8. Electrochemical characterization of GaN surface states

    Science.gov (United States)

    Winnerl, Andrea; Garrido, Jose A.; Stutzmann, Martin

    2017-07-01

    In this work, we present a systematic study of the electrochemical properties of metal-organic chemical vapor deposition and hybrid vapor phase epitaxy grown n-type GaN in aqueous electrolytes. For this purpose, we perform cyclic voltammetry and impedance spectroscopy measurements over a wide range of potentials and frequencies, using a pure aqueous electrolyte and adding two different types of redox couples, as well as applying different surface treatments to the GaN electrodes. For Ga-polar GaN electrodes, the charge transfer to an electrolyte is dominated by surface states, which are not related to dislocations and are independent of the specific growth technique. These surface states can be modified by the surface treatment; they are generated by etching in HCl and are passivated by oxidation. Different surface defect states are present on N-polar GaN electrodes which do not significantly contribute to the charge transfer across the GaN/electrolyte interface.

  9. Electrochemical surface modification technique to impede mild steel corrosion using perfluorooctanoic acid

    Directory of Open Access Journals (Sweden)

    Shubha H Natarj

    2016-02-01

    Full Text Available The present work demonstrated that corrosion inhibition efficiency of electrochemically generated organic coat is remarkably effective than self-assembled monolayer (SAM generated by dip coating technique. Perfluorooctanoic Acid (PFOA is used to modify mild steel surface for effective protection. Infrared reflection absorption spectroscopy and contact angle measurements substantiate the modification of mild steel surface and its effect on surface hydrophobicity. A comparison between electrochemical properties of PFOA SAM generated by dip coat method (DC-PFOA and PFOA coat generated by electrochemical method (EC-PFOA is presented. Electrochemical measurements reveal that the corrosion protection efficiency of EC-PFOA (91% is much superior to DC-PFOA (28%.

  10. Mechanism of glucose electrochemical oxidation on gold surface

    KAUST Repository

    Pasta, Mauro

    2010-08-01

    The complex oxidation of glucose at the surface of gold electrodes was studied in detail in different conditions of pH, buffer and halide concentration. As observed in previous studies, an oxidative current peak occurs during the cathodic sweep showing a highly linear dependence on glucose concentration, when other electrolyte conditions are unchanged. The effect of the different conditions on the intensity of this peak has stressed the limitations of the previously proposed mechanisms. A mechanism able to explain the presence of this oxidative peak was proposed. The mechanism takes into account ion-sorption and electrochemical adsorption of OH-, buffer species (K2HPO4/KH2PO4) and halides. © 2010 Elsevier Ltd. All rights reserved.

  11. Three-dimensional polypyrrole-derived carbon nanotube framework for dye adsorption and electrochemical supercapacitor

    Energy Technology Data Exchange (ETDEWEB)

    Xin, Shengchang; Yang, Na; Gao, Fei [School of Life Sciences, State Key Laboratory of Coordination Chemistry and Collaborative Innovation Center of Chemistry for Life Sciences, Institute of Chemistry and BioMedical Sciences, Nanjing University, Nanjing 210093 (China); Zhao, Jing, E-mail: jingzhao@nju.edu.cn [School of Life Sciences, State Key Laboratory of Coordination Chemistry and Collaborative Innovation Center of Chemistry for Life Sciences, Institute of Chemistry and BioMedical Sciences, Nanjing University, Nanjing 210093 (China); Li, Liang, E-mail: msell08@163.com [School of Materials Science and Engineering, Wuhan Institute of Technology, Wuhan 430073 (China); Teng, Chao, E-mail: tengc@pkusz.edu.cn [Guangdong Provincial Key Laboratory of Nano-Micro Materials Research, School of Chemical Biology & Biotechnology, Peking University Shenzhen Graduate School, Shenzhen 518055 (China)

    2017-08-31

    Highlights: • Three-dimensional polypyrrole-derived carbon nanotube frameworks are prepared. • They display outstanding absorption capacity (609 mg g{sup −1}) towards methylene blue. • They possess high specific capacitance (167 F g{sup −1}) and good rate capability (64%). • They have excellent cycling performance with no capacitance loss over 1000 cycles. - Abstract: Three-dimensional carbon nanotube frameworks have been prepared via pyrolysis of polypyrrole nanotube aerogels that are synthesized by the simultaneous self-degraded template synthesis and hydrogel assembly followed by freeze-drying. The microstructure and composition of the materials are investigated by thermal gravimetric analysis, Raman spectrum, X-ray photoelectron spectroscopy, transmission electron microscopy, and specific surface analyzer. The results confirm the formation of three-dimensional carbon nanotube frameworks with low density, high mechanical properties, and high specific surface area. Compared with PPy aerogel precursor, the as-prepared three-dimensional carbon nanotube frameworks exhibit outstanding adsorption capacity towards organic dyes. Moreover, electrochemical tests show that the products possess high specific capacitance, good rate capability and excellent cycling performance with no capacitance loss over 1000 cycles. These characteristics collectively indicate the potential of three-dimensional polypyrrole-derived carbon nanotube framework as a promising macroscopic device for the applications in environmental and energy storages.

  12. Characterizing electrocatalytic surfaces: Electrochemical and NMR studies of methanol and carbon monoxide on Pt/C

    Energy Technology Data Exchange (ETDEWEB)

    McGrath, Patrick; Fojas, Aurora Marie; Rush, Benjamin; Reimer, Jeffrey A.; Cairns, Elton J. [Lawrence Berkeley National Laboratory and University of California, Berkeley, CA 94720 (United States)

    2007-12-20

    We use cyclic voltammetry (CV) on fuel cell electrodes to elucidate the important differences between adsorbates resulting from carbon monoxide adsorption and methanol adsorption onto commercial Pt/C electrocatalysts in a sulfuric acid electrolyte. Under open circuit conditions, methanol was found to adsorb preferentially onto the Pt sites associated with 'strongly bound' hydrogen. The sites associated with 'weakly bound' hydrogen adsorbed methanol more slowly. In the case of CO adsorption, which requires no adsorbate dehydrogenation, all adsorption sites showed similar affinity towards the adsorbate. Electrochemical oxidation of the adsorbates derived from both methanol and CO exposure exhibit slower oxidation when the adsorbate is associated with cubic-packed-like sites than from close-packed-steps and other sites. NMR of a {sup 13}CO-adlayer prepared by electrochemical adsorption from low concentration {sup 13}CH{sub 3}OH shows a lower NMR shift and smaller linewidth than the previously reported values for electrochemically adsorbed {sup 13}CO gas. These results are interpreted in terms of adsorbate motion on the electrocatalyst surface. (author)

  13. Diamond surface functionalization with biomimicry - Amine surface tether and thiol moiety for electrochemical sensors

    Science.gov (United States)

    Sund, James B.; Causey, Corey P.; Wolter, Scott D.; Parker, Charles B.; Stoner, Brian R.; Toone, Eric J.; Glass, Jeffrey T.

    2014-05-01

    The surface of conducting diamond was functionalized with a terminal thiol group that is capable of binding and detecting nitrogen-oxygen species. The functionalization process employed multiple steps starting with doped diamond films grown by plasma enhanced chemical vapor deposition followed by hydrogen termination and photochemical attachment of a chemically protected amine alkene. The surface tether was deprotected to reveal the amine functionality, which enabled the tether to be extended with surface chemistry to add a terminal thiol moiety for electrochemical sensing applications. Each step of the process was validated using X-ray photoelectron spectroscopy analysis.

  14. Diamond surface functionalization with biomimicry – Amine surface tether and thiol moiety for electrochemical sensors

    Energy Technology Data Exchange (ETDEWEB)

    Sund, James B., E-mail: jim@jamessund.com [Department of Electrical and Computer Engineering, Duke University, Durham, NC (United States); Causey, Corey P. [Departments of Chemistry and Biochemistry, Duke University, Durham, NC (United States); Wolter, Scott D. [Department of Physics, Elon University, Elon, NC 27244 (United States); Parker, Charles B., E-mail: charles.parker@duke.edu [Department of Electrical and Computer Engineering, Duke University, Durham, NC (United States); Stoner, Brian R. [Department of Electrical and Computer Engineering, Duke University, Durham, NC (United States); Research Triangle Institute (RTI) International, Research Triangle Park, NC (United States); Toone, Eric J. [Departments of Chemistry and Biochemistry, Duke University, Durham, NC (United States); Glass, Jeffrey T. [Department of Electrical and Computer Engineering, Duke University, Durham, NC (United States)

    2014-05-01

    Highlights: • Diamond surfaces were functionalized with organic molecules using a novel approach. • Used biomimicry to select a molecule to bind NO, similar to the human body. • Molecular orbital theory predicted the molecule-analyte oxidation behavior. • A thiol moiety was attached to an amine surface tether on the diamond surface. • XPS analysis verified each surface functionalization step. - Abstract: The surface of conducting diamond was functionalized with a terminal thiol group that is capable of binding and detecting nitrogen–oxygen species. The functionalization process employed multiple steps starting with doped diamond films grown by plasma enhanced chemical vapor deposition followed by hydrogen termination and photochemical attachment of a chemically protected amine alkene. The surface tether was deprotected to reveal the amine functionality, which enabled the tether to be extended with surface chemistry to add a terminal thiol moiety for electrochemical sensing applications. Each step of the process was validated using X-ray photoelectron spectroscopy analysis.

  15. Investigation on electrochemical behavior and its catalytic effect on oxygen reduction reaction of 3-Ferrocenyl dihydropyrazole derivative as electron relay

    Science.gov (United States)

    Zeng, Han; Huo, Wen-Shan; Zhao, Shu-Xian; Zhang, Yu-He

    2017-11-01

    Amino group surface tailored multi-wall carbon nano-tubes were covalently tethered to the gold disk electrode and Laccase molecules were covalently coupled to nano-tubes to prepare Lac-based electrode. Derivative of 3-ferrocenyl dihydropyrazole (FDPFFP) was proposed to be electron mediator for mediated oxygen reduction reaction. Investigation in electro-chemical behavior and catalytic performance to enzymatic reaction of FDPFFP indicated that it displayed quasi-reversible characteristics of electro-chemical reaction with rapid dynamics of electron shuttle and had apparent catalytic effect in oxygen reduction (onset potential for catalysis at 450 mV vs NHE). This enzymatic catalysis was restrained by the step in diffusion of substrate.

  16. Urethane tetrathiafulvalene derivatives: synthesis, self-assembly and electrochemical properties

    Directory of Open Access Journals (Sweden)

    Xiang Sun

    2015-11-01

    Full Text Available This paper reports the self-assembly of two new tetrathiafulvalene (TTF derivatives that contain one or two urethane groups. The formation of nanoribbons was evidenced by scanning electron microscopy (SEM and X-ray diffraction (XRD, which showed that the self-assembly ability of T1 was better than that of T2. The results revealed that more urethane groups in a molecule did not necessarily instigate self-assembly. UV–vis and FTIR spectra were measured to explore noncovalent interactions. The driving forces for self-assembly of TTF derivatives were mainly hydrogen bond interactions and π–π stacking interactions. The electronic conductivity of the T1 and T2 films was tested by a four-probe method.

  17. Silicon Carbide-Derived Carbon Prepared by Fused Salt Electrolysis and Electrochemical Performance

    Directory of Open Access Journals (Sweden)

    Shuyuan Wang

    2016-01-01

    Full Text Available A number of carbide-derived carbon (CDC samples were successfully synthesized by the electrolysis of SiC powder in molten CaCl2. The electrolysis was conducted at different temperatures (850, 900, and 950°C for 48 h in argon at an applied constant voltage of 3.1 V. The structure of the resulting carbon is characterized by X-ray diffraction, Raman spectroscopy, and transmission electron microscope techniques. Cyclic voltammetry and galvanostatic charge/discharge measurements are applied to investigate electrochemical performances of the SiC-CDC material. It can be seen that the degree of order of the SiC-CDC increases monotonically along with elevation of reaction temperature, while the highest specific surface area 1137.74 m2/g together with a specific capacitance of 161.27 F/g at a current density 300 mA/g was achieved from sample synthesized at 900°C.

  18. Preparation of superhydrophobic titanium surfaces via electrochemical etching and fluorosilane modification

    Energy Technology Data Exchange (ETDEWEB)

    Lu Yao [School of Mechanical Engineering, Dalian University of Technology, Dalian 116024 (China); Xu Wenji, E-mail: wenjixu@dlut.edu.cn [School of Mechanical Engineering, Dalian University of Technology, Dalian 116024 (China); Song Jinlong; Liu Xin; Xing Yingjie; Sun Jing [School of Mechanical Engineering, Dalian University of Technology, Dalian 116024 (China)

    2012-12-15

    Highlights: Black-Right-Pointing-Pointer We prepare superhydrophobic titanium surfaces via electrochemical etching and fluorosilane modification that have stability and abrasion resistance. Black-Right-Pointing-Pointer Ion activities take place in neutral solution can drive Ti dissolution without affecting the pH. Black-Right-Pointing-Pointer Analysis of the electrolyte, reaction process, and products indicates that the electrochemical processing is harmless and environment-friendly. - Abstract: The preparation of superhydrophobic surfaces on hydrophilic metal substrates depends on both surface microstructures and low surface energy modification. In this study, a simple and inexpensive electrochemical method for preparing robust superhydrophobic titanium surfaces is reported. The neutral sodium chloride solution is used as electrolyte. Fluoroalkylsilane (FAS) was used to reduce the surface energy of the electrochemically etched surface. Scanning electron microscopy (SEM) images, energy-dispersive spectroscopy (EDS), Fourier transform infrared spectroscopy (FTIR) spectra, and contact angle measurement are performed to characterize the morphological features, chemical composition, and wettability of the titanium surfaces. Stability and friction tests indicate that the prepared titanium surfaces are robust. The analysis of electrolyte, reaction process, and products demonstrates that the electrochemical processing is very inexpensive and environment-friendly. This method is believed to be easily adaptable for use in large-scale industry productions to promote the application of superhydrophobic titanium surfaces in aviation, aerospace, shipbuilding, and the military industry.

  19. Investigation of adsorption of isoniazid derivatives at mild steel/hydrochloric acid interface: Electrochemical and weight loss methods

    Energy Technology Data Exchange (ETDEWEB)

    Singh, Ashish Kumar [Department of Applied Chemistry, Institute of Technology Banaras Hindu University, Varanasi 221 005 (India); Quraishi, M.A., E-mail: maquraishi.apc@itbhu.ac.in [Department of Applied Chemistry, Institute of Technology Banaras Hindu University, Varanasi 221 005 (India)

    2010-10-01

    The corrosion inhibition properties of isoniazid derivatives, namely N-(morpholino methyl) isatin-3-isonicotinoyl hydrazone (MIIH), N-(piperazino methyl) isatin-3-isonicotinoyl hydrazone (PIIH), N-(2-Thio benzimidazolyl methyl) isatin-3-isonicotinoyl hydrazone (TBIH), N-(piperadino methyl) isatin-3-isonicotinoyl hydrazone (PIIIH) for mild steel corrosion in 1 M HCl medium were analysed by electrochemical impedance spectroscopy (EIS), potentiodynamic polarization and weight loss techniques. Electrochemical impedance data demonstrated that the addition of the isoniazid derivatives in the corrosive solution decreased the charge capacitance and simultaneously increased the function of the charge/discharge of the interface, facilitating the formation of an adsorbed layer over the steel surface. Adsorption of these inhibitors on the steel surface obeyed the Langmuir adsorption isotherm. Potentiodynamic polarization studies showed that all the tested inhibitors affected both the anodic and cathodic process, thus they can be classified as mixed type of inhibitor. The effect of chemical structure of the four tested inhibitors was discussed. It was found that the efficiency order followed by molecules tested was TBIH > PIIH > MIIH > PIIIH. Thus TBIH turned out to be the best inhibitor. This fact strongly suggests that, an efficient corrosion inhibitor molecule should be large one, planar, having unoccupied d-orbital and also containing an extensive number of {pi}-electrons.

  20. Carbide-Derived Carbon Films for Integrated Electrochemical Energy Storage

    Science.gov (United States)

    Heon, Min

    Active RFID tags, which can communicate over tens or even hundreds of meters, MEMS devices of several microns in size, which are designed for the medical and pharmaceutical purposes, and sensors working in wireless monitoring systems, require microscale power sources that are able to provide enough energy and to satisfy the peak power demands in those applications. Supercapacitors have not been an attractive candidate for micro-scale energy storage, since most nanoporous carbon electrode materials are not compatible with micro-fabrication techniques and have failed to meet the requirements of high volumetric energy density and small form factor for power supplies for integrated circuits or microelectronic devices or sensors. However, supercapacitors can provide high power density, because of fast charging/discharging, which can enable self-sustaining micro-modules when combined with energy-harvesting devices, such as solar cell, piezoelectric or thermoelectric micro-generators. In this study, carbide-derived carbon (CDC) films were synthesized via vacuum decomposition of carbide substrates and gas etching of sputtered carbide thin films. This approach allowed manufacturing of porous carbon films on SiC and silicon substrates. CDC films were studied for micro-supercapacitor electrodes, and showed good double layer capacitance. Since the gas etching technique is compatible with conventional micro-device fabrication processes, it can be implemented to manufacture integrated on-chip supercapacitors on silicon wafers.

  1. Cauliflower-derived porous carbon without activation for electrochemical capacitor and CO2 capture applications

    Science.gov (United States)

    Du, Juan; Yu, Yifeng; Lv, Haijun; Chen, Chunlin; Zhang, Jian; Chen, Aibing

    2018-01-01

    Carbon materials have attracted great attention in CO2 capture and energy storage due to their excellent characteristics such as tunable pore structure, modulated surface properties and superior bulk conductivities, etc. Biomass, provided by nature with non-toxic, widespread, abundant, and sustainable advantages, is considered to be a very promising precursor of carbons for the view of economic, environmental, and societal issues. However, the preparation of high-performance biomass-derived carbons is still a big challenge because of the multistep process for their synthesis and subsequent activation. Herein, hierarchically porous structured carbon materials have been prepared by directly carbonizing dried cauliflowers without any addition of agents and activation process, featuring with large specific surface area, hierarchically porous structure and improved pore volume, as well as suitable nitrogen content. Being used as a solid-state CO2 adsorbent, the obtained product exhibited a high CO2 adsorption capacity of 3.1 mmol g-1 under 1 bar and 25 °C and a remarkable reusability of 96.7% retention after 20 adsorption/regeneration cycles. Our study reveals that choosing a good biomass source was significant as the unique structure of precursor endows the carbonized product with abundant pores without the need of any post-treatment. Used as an electrode material in electrochemical capacitor, the non-activated porous carbon displayed a fairly high specific capacitance of 228.9 F g-1 at 0.5 A g-1 and an outstanding stability of 99.2% retention after 5000 cycles at 5 A g-1. [Figure not available: see fulltext.

  2. Electrochemical carbon dioxide reduction on rough copper surfaces

    NARCIS (Netherlands)

    Kas, Recep

    2016-01-01

    Sustainable development and climate change is considered to be one of the top challenges of humanity. Electrochemical carbon dioxide (CO2) reduction to fuels or fuel precursor using renewable electricity is a very promising way to recycle CO2 and store the electricity. This would also provide

  3. Surface and Electrochemical Properties of Polymer Brush-Based Redox Poly(Ionic Liquid).

    Science.gov (United States)

    Bui-Thi-Tuyet, Van; Trippé-Allard, Gaëlle; Ghilane, Jalal; Randriamahazaka, Hyacinthe

    2016-10-26

    Redox-active poly(ionic liquid) poly(3-(2-methacryloyloxy ethyl)-1-(N-(ferrocenylmethyl) imidazolium bis(trifluoromethylsulfonyl)imide deposited onto electrode surfaces has been prepared using surface-initiated atom transfer radical polymerization SI-ATRP. The process starts by electrochemical immobilization of initiator layer, and then methacrylate monomer carrying ferrocene and imidazolium units is polymerized in ionic liquid media via SI-ATRP process. The surfaces analyses of the polymer exhibit a well-defined polymer brushlike structure and confirm the presence of ferrocene and ionic moieties within the film. Furthermore, the electrochemical investigations of poly(redox-active ionic liquid) in different media demonstrate that the electron transfer is not restricted by the rate of counterion migration into/out of the polymer. The attractive electrochemical performance of these materials is further demonstrated by performing electrochemical measurement, of poly(ferrocene ionic liquid), in solvent-free electrolyte. The facile synthesis of such highly ordered electroactive materials based ionic liquid could be useful for the fabrication of nanostructured electrode suitable for performing electrochemistry in solvent free electrolyte. We also demonstrate possible applications of the poly(FcIL) as electrochemically reversible surface wettability system and as electrochemical sensor for the catalytic activity toward the oxidation of tyrosine.

  4. Nanoscale electrochemical patterning reveals the active sites for catechol oxidation at graphite surfaces.

    Science.gov (United States)

    Patel, Anisha N; McKelvey, Kim; Unwin, Patrick R

    2012-12-19

    Graphite-based electrodes (graphite, graphene, and nanotubes) are used widely in electrochemistry, and there is a long-standing view that graphite step edges are needed to catalyze many reactions, with the basal surface considered to be inert. In the present work, this model was tested directly for the first time using scanning electrochemical cell microscopy reactive patterning and shown to be incorrect. For the electro-oxidation of dopamine as a model process, the reaction rate was measured at high spatial resolution across a surface of highly oriented pyrolytic graphite. Oxidation products left behind in a pattern defined by the scanned electrochemical cell served as surface-site markers, allowing the electrochemical activity to be correlated directly with the graphite structure on the nanoscale. This process produced tens of thousands of electrochemical measurements at different locations across the basal surface, unambiguously revealing it to be highly electrochemically active, with step edges providing no enhanced activity. This new model of graphite electrodes has significant implications for the design of carbon-based biosensors, and the results are additionally important for understanding electrochemical processes on related sp(2)-hybridized materials such as pristine graphene and nanotubes.

  5. Facile preparation of self-healing superhydrophobic CeO2 surface by electrochemical processes

    Science.gov (United States)

    Nakayama, Katsutoshi; Hiraga, Takuya; Zhu, Chunyu; Tsuji, Etsushi; Aoki, Yoshitaka; Habazaki, Hiroki

    2017-11-01

    Herein we report simple electrochemical processes to fabricate a self-healing superhydrophobic CeO2 coating on Type 304 stainless steel. The CeO2 surface anodically deposited on flat stainless steel surface is hydrophilic, although high temperature-sintered and sputter-deposited CeO2 surface was reported to be hydrophobic. The anodically deposited hydrophilic CeO2 surface is transformed to hydrophobic during air exposure. Specific accumulation of contaminant hydrocarbon on the CeO2 surface is responsible for the transformation to hydrophobic state. The deposition of CeO2 on hierarchically rough stainless steel surface produces superhydrophobic CeO2 surface, which also shows self-healing ability; the surface changes to superhydrophilic after oxygen plasma treatment but superhydrophobic state is recovered repeatedly by air exposure. This work provides a facile method for preparing a self-healing superhydrophobic surface using practical electrochemical processes.

  6. Electrochemical modification of gold electrodes with azobenzene derivatives by diazonium reduction.

    Science.gov (United States)

    Kibena, Elo; Marandi, Margus; Mäeorg, Uno; Venarusso, Luna B; Maia, Gilberto; Matisen, Leonard; Kasikov, Aarne; Sammelselg, Väino; Tammeveski, Kaido

    2013-04-02

    An electrochemical study of Au electrodes electrografted with azobenzene (AB), Fast Garnet GBC (GBC) and Fast Black K (FBK) diazonium compounds is presented. Electrochemical quartz crystal microbalance, ellipsometry and atomic force microscopy investigations reveal the formation of multilayer films. The elemental composition of the aryl layers is examined by X-ray photoelectron spectroscopy. The electrochemical measurements reveal a quasi-reversible voltammogram of the Fe(CN)6 (3-/4-) redox couple on bare Au and a sigmoidal shape for the GBC- and FBK-modified Au electrodes, thus demonstrating that electron transfer is blocked due to the surface modification. The electrografted AB layer results in strongest inhibition of the Fe(CN)6 (3-/4-) response compared with other aryl layers. The same tendencies are observed for oxygen reduction; however, the blocking effect is not as strong as in the Fe(CN)6 (3-/4-) redox system. The electrochemical impedance spectroscopy measurements allowed the calculation of low charge-transfer rates to the Fe(CN)6 (3-) probe for the GBC- and FBK-modified Au electrodes in relation to bare Au. From these measurements it can be concluded that the FBK film is less compact or presents more pinholes than the electrografted GBC layer. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  7. Electrochemical removal of segregated silicon dioxide impurities from yttria stabilized zirconia surfaces at elevated temperatures

    DEFF Research Database (Denmark)

    Andersen, Thomas; Hansen, Karin Vels; Mogensen, Mogens Bjerg

    2011-01-01

    Here we report on the electrochemical removal of segregated silicon dioxide impurities from Yttria Stabilized Zirconia (YSZ) surfaces at elevated temperatures studied under Ultra High Vacuum (UHV) conditions. YSZ single crystals were heated in vacuum by an applied 18kHz a.c. voltage using the ionic...... electrochemically reduced by the a.c. voltage when no oxidation substances are present. The absence of silicon on the surfaces annealed in vacuum or at low oxygen or water vapor partial pressures was attributed to electrochemical reduction of silicon dioxide to volatile silicon monoxide on the YSZ surface....... This was demonstrated by silicon enrichment of a gold foil placed behind the YSZ crystal surface while annealed. The results suggest a fast way to clean YSZ for trace silicon dioxide impurities found in the bulk of the cleanest crystals commercially available....

  8. A study of electrodischarge machining–pulse electrochemical machining combined machining for holes with high surface quality on superalloy

    Directory of Open Access Journals (Sweden)

    Ning Ma

    2015-11-01

    Full Text Available Noncircular holes on the surface of turbine rotor blades are usually machined by electrodischarge machining. A recast layer containing numerous micropores and microcracks is easily generated during the electrodischarge machining process due to the rapid heating and cooling effects, which restrict the wide applications of noncircular holes in aerospace and aircraft industries. Owing to the outstanding advantages of pulse electrochemical machining, electrodischarge machining–pulse electrochemical machining combined technique is provided to improve the overall quality of electrodischarge machining-drilled holes. The influence of pulse electrochemical machining processing parameters on the surface roughness and the influence of the electrodischarge machining–pulse electrochemical machining method on the surface quality and accuracy of holes have been studied experimentally. The results indicate that the pulse electrochemical machining processing time for complete removal of the recast layer decreases with the increase in the pulse electrochemical machining current. The low pulse electrochemical machining current results in uneven dissolution of the recast layer, while the higher pulse electrochemical machining current induces relatively homogeneous dissolution. The surface roughness is reduced from 4.277 to 0.299 µm, and the hole taper induced by top-down electrodischarge machining process was reduced from 1.04° to 0.17° after pulse electrochemical machining. On account of the advantages of electrodischarge machining and the pulse electrochemical machining, the electrodischarge machining–pulse electrochemical machining combined technique could be applied for machining noncircular holes with high shape accuracy and surface quality.

  9. Surface electrochemical control for fine coal and pyrite separation. Technical progress report, July 1, 1991--September 30, 1991

    Energy Technology Data Exchange (ETDEWEB)

    Hu, Weibai; Huang, Qinping; Li, Jun; Riley, A.; Turcotte, S.B.; Benner, R.E.; Zhu, Ximeng; Bodily, D.M.; Liang, Jun; Zhong, Tinghe; Wadsworth, M.E.

    1991-12-31

    The ongoing work includes the characterization of coal pyrites, the floatability evaluation of three typical US coal samples, the flotation behavior of coal pyrites, the electrochemical measurement of the surface properties of coal pyrites, and the characterization of species produced at pyrite surfaces. This report covers a Raman spectroscopy of species produced electrochemically on pyrite surfaces.

  10. Synthesis of metal-semiconductor core-shell nanoparticles using electrochemical surface-limited reactions.

    Science.gov (United States)

    Gu, Chaokang; Xu, Hui; Park, Minseo; Shannon, Curtis

    2009-01-06

    We report the synthesis of Au/CuI and Au/CdS core-shell nanoparticle (NP) thin films using codeposition and electrochemical atomic layer deposition (EC-ALD). Au nanoparticle films were prepared on glassy carbon supports by depositing alternating layers of poly(diallyl dimethylammonium)-stabilized Au nanoparticles and CoP(2)W(17)O(61)(8-) polyoxometallate interlayers. From there, CuI was deposited onto the surface of Au nanoparticles using electrochemical atomic layer deposition, while CdS films were grown by an atom-by-atom codeposition method. The semiconductor-Au core-shell nanoparticles were characterized by electrochemistry, photoluminescence spectroscopy, and Raman spectroscopy. Our results indicate that the semiconductors deposit onto the AuNP surface by surface limited electrochemical reactions.

  11. Evaluation Of Electrochemical Machining Technology For Surface Improvements In Additive Manufactured Components

    Energy Technology Data Exchange (ETDEWEB)

    Dehoff, Ryan R [ORNL; List III, Frederick Alyious [ORNL; Carver, Keith [ORNL

    2015-09-23

    ORNL Manufacturing Demonstration Facility worked with ECM Technologies LLC to investigate the use of precision electro-chemical machining technology to polish the surface of parts created by Arcam electron beam melting. The goals for phase one of this project have been met. The project goal was to determine whether electro-chemical machining is a viable method to improve the surface finish of Inconel 718 parts fabricated using the Arcam EBM method. The project partner (ECM) demonstrated viability for parts of both simple and complex geometry. During the course of the project, detailed process knowledge was generated. This project has resulted in the expansion of United States operations for ECM Technologies.

  12. Friction Reduction of Chrome-Coated Surface with Micro-Dimple Arrays Generated by Electrochemical Micromachining

    Science.gov (United States)

    Chen, Xiaolei; Qu, Ningsong; Hou, Zhibao; Wang, Xiaolei; Zhu, Di

    2017-02-01

    Surface coating and surface texture play a significant role in enhancing the tribological properties of mechanical components. In this study, to further improve the tribological properties of a chrome-coated surface, arrays of circular- and square-shaped micro-dimples were generated on chrome-coated surfaces via electrochemical machining. Through-mask electrochemical micromachining (TMEMM) is a popular electrochemical micromachining method for generating micro-dimple arrays. However, photolithography is a necessary process in conventional TMEMM before electrochemical micromachining, which is time-consuming and expensive when used in mass production. A reusable polydimethylsiloxane mask was introduced to prepare the micro-dimples. Circular micro-dimples of 120 μm diameter and square micro-dimples of 106 μm side length were fabricated on a chrome-coated surface. The results of friction tests indicated that at a load of 220 N, 10 μm deep micro-dimples reduced the coefficient of friction (CoF) significantly compared to an untextured surface. At a load of 320 and 420 N, the CoF continually decreased when the depth of the micro-dimples was increased from 0 to 20 μm. In addition, the results showed that, compared to circular micro-dimples, square micro-dimples contributed to a higher friction reduction ratio under the same conditions. The best friction reduction ratio was found for square dimples with a depth of 20 μm.

  13. 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.

  14. Controlled amino-functionalization by electrochemical reduction of bromo and nitro azobenzene layers bound to Si(111) surfaces.

    Science.gov (United States)

    Ullien, Daniela; Thüne, Peter C; Jager, Wolter F; Sudhölter, Ernst J R; de Smet, Louis C P M

    2014-09-28

    4-Nitrobenzenediazonium (4-NBD) and 4-bromobenzenediazonium (4-BBD) salts were grafted electrochemically onto H-terminated, p-doped silicon (Si) surfaces. Atomic force microscopy (AFM) and ellipsometry experiments clearly showed layer thicknesses of 2-7 nm, which indicate multilayer formation. Decreasing the diazonium salt concentration and the reaction time resulted in a smaller layer thickness, but did not prevent the formation of multilayers. It was demonstrated, mainly by X-ray photoelectron spectroscopy (XPS), that the diazonium salts not only react with the H-terminated Si surface, but also with electrografted phenyl groups via azo-bond formation. These azo bonds can be electrochemically reduced at Ered = -1.5 V, leading to the corresponding amino groups. This reduction resulted in a modest decrease in layer thickness, and did not yield monolayers. This indicates that other coupling reactions, notably a biphenyl coupling, induced by electrochemically produced phenyl radicals, take place as well. In addition to the azo functionalities, the nitro functionalities in electrografted layers of 4-NBD were independently reduced to amino functionalities at a lower potential (Ered = -2.1 V). The presence of amino functionalities on fully reduced layers, both from 4-NBD- and 4-BBD-modified Si, was shown by the presence of fluorine after reaction with trifluoroacetic anhydride (TFAA). This study shows that the electrochemical reduction of azo bonds generates amino functionalities on layers produced by electrografting of aryldiazonium derivatives. In this way multifunctional layers can be formed by employing functional aryldiazonium salts, which is believed to be very practical in the fabrication of sensor platforms, including those made of multi-array silicon nanowires.

  15. Green synthesis of 1,4-quinone derivatives and evaluation of their fluorescent and electrochemical properties

    Directory of Open Access Journals (Sweden)

    Palanisamy Ravichandiran

    2016-09-01

    Full Text Available Green synthesis of some 1,4-quinone derivatives by conventional and solvent free microwave assisted methods has been reported. The microwave assisted method resulted in higher percentage yield at shorter time compared to the conventional one. In the conventional method environmentally friendly solvent was used and the results were compared with other solvents. When water was used as a solvent the reaction exhibited higher yield than other solvents like ethanol. The solvent free method under microwave irradiation method yielded the highest yield compared to the conventional methods. The resultant compounds were analyzed by UV–Vis, FT-IR, 1H and 13C NMR spectroscopy. The synthesized quinone derivatives exhibited the fluorescent and electrochemical properties.

  16. Fabrication of microlens array on silicon surface using electrochemical wet stamping technique

    Science.gov (United States)

    Lai, Lei-Jie; Zhou, Hang; Zhu, Li-Min

    2016-02-01

    This paper focuses on the fabrication of microlens array (MLA) on silicon surface by taking advantage of a novel micromachining approach, the electrochemical we stamping (E-WETS). The E-WETS allows the direct imprinting of MLA on an agarose stamp into the substrate through a selective anodic dissolution process. The pre-patterned agarose stamp can direct and supply the solution preferentially on the contact area between the agarose stamp and the substrate, to which the electrochemical reaction is confined. The anodic potential vs. saturated calomel electrode is optimized and 1.5 V is chosen as the optimum value for the electrochemical polishing of p-Si. A refractive MLA on a PMMA mold is successfully transferred onto the p-Si surface. The machining deviations of the fabricated MLA from those on the mold are 0.44% in diameter and 2.1% in height respectively, and the machining rate in HF is around 1.1 μm/h. The surface roughness of the fabricated MLA is less than 12 nm owing to the electrochemical polishing process. The results demonstrate that E-WETS is a promising approach to fabricate MLA on p-Si surface with high accuracy and efficiency.

  17. Control of interpenetration of copper-based MOFs on supported surfaces by electrochemical synthesis

    NARCIS (Netherlands)

    Sachdeva, S.; Pustovarenko, A.; Sudhölter, E.J.R.; Kapteijn, F.; De Smet, L.C.P.M.; Gascon, J.

    2016-01-01

    A study of a copper-based metal–organic framework (MOF) synthesized by an electrochemical route is presented. Morphological and adsorption properties of the MOF synthesized as bulk powder and on supported copper surfaces were investigated. Differences in these properties and structural refinement

  18. Electrochemical and quantum chemical studies of some indole derivatives as corrosion inhibitors for C38 steel in molar hydrochloric acid

    Energy Technology Data Exchange (ETDEWEB)

    Lebrini, M. [Laboratoire Materiaux et Molecules en Milieu Amazonien, CNRS 8172-UMR ECOFOG, Campus Trou Biran, Cayenne 97337, French Guiana (France); Robert, F. [Laboratoire Materiaux et Molecules en Milieu Amazonien, UAG-UMR ECOFOG, Campus Trou Biran, Cayenne 97337, French Guiana (France); Vezin, H. [Laboratoire de Chimie Organique et Macromoleculaire, UMR-CNRS 8009, USTL BatC4 F-59655 Villeneuve d' Ascq Cedex (France); Roos, C., E-mail: christophe.roos@guyane.univ-ag.f [Laboratoire Materiaux et Molecules en Milieu Amazonien, UAG-UMR ECOFOG, Campus Trou Biran, Cayenne 97337, French Guiana (France)

    2010-10-15

    A comparative study of 9H-pyrido[3,4-b]indole (norharmane) and 1-methyl-9H-pyrido[3,4-b]indole (harmane) as inhibitors for C38 steel corrosion in 1 M HCl solution at 25 {sup o}C was carried out. Potentiodynamic polarization and electrochemical impedance spectroscopy (EIS) techniques were applied to study the metal corrosion behavior in the absence and presence of different concentrations of these inhibitors. The OCP as a function of time were also established. Cathodic and anodic polarization curves show that norharmane and harmane are a mixed-type inhibitors. Adsorption of indole derivatives on the C38 steel surface, in 1 M HCl solution, follows the Langmuir adsorption isotherm model. The {Delta}G{sub ads}{sup o} values were calculated and discussed. The potential of zero charge (PZC) of the C38 steel in inhibited solution was studied by the EIS method, and a mechanism for the adsorption process was proposed. Raman spectroscopy confirmed that indole molecules strongly adsorbed onto the steel surface. The electronic properties of indole derivates, obtained using the AM1 semi-empirical quantum chemical approach, were correlated with their experimental efficiencies using the linear resistance model (LR).

  19. A silk derived carbon fiber mat modified with Au@Pt urchilike nanoparticles: A new platform as electrochemical microbial biosensor.

    Science.gov (United States)

    Deng, Liu; Guo, Shaojun; Zhou, Ming; Liu, Ling; Liu, Chang; Dong, Shaojun

    2010-06-15

    We present here a facile and efficient route to prepare silk derived carbon mat modified with Au@Pt urchilike nanoparticles (Au@Pt NPs) and develop an Escherichia coli (E. coli)-based electrochemical sensor using this material. Silk is a natural protein fiber, and it is abundant with kinds of functionalities which are important in the development of the derived material. The S-derived carbon fiber mat have amino, pyridine and carbonyl functional groups, these natural existent functionalities allow the Au@Pt NPs to self-assemble on the carbon fiber surface and provide a biocompatible microenvironment for bacteria. The Au@Pt NPs modified S-derived carbon fiber is sensitive to detect the E. coli activities with a low detection limit, where glucose is used as a prelimiltary substrate to evaluate them. The performance of Au@Pt/carbon fiber mat based biosensor is much better than that of commercial carbon paper based biosensor. The high sensitivity of this biosensor stems from the unique electrocatalytic properties of Au@Pt urchilike NPs and quinone groups presented in S-derived carbon fiber. This biosensor is also tested for detection of organophosphate pesticides, fenamiphos. The relative inhibition of E. coli activity is linear with -log[fenamiphos] at the concentration range from 0.5mg/L to 36.6 mg/L with lowest observable effect concentration (LOEC) of 0.09 mg/L. The Au@Pt NPs modified S-derived carbon fiber mat possesses high conductivity, biocompatibility and high electrocatalytic activity and be can used as advanced electrode materials for microbial biosensor improvement. The microbial biosensor based on this material shows potential applications in environmental monitoring. Copyright 2010 Elsevier B.V. All rights reserved.

  20. Reversible Compositional Control of Oxide Surfaces by Electrochemical Potentials

    KAUST Repository

    Mutoro, Eva

    2012-01-05

    Perovskite oxides can exhibit a wide range of interesting characteristics such as being catalytically active and electronically/ionically conducting, and thus, they have been used in a number of solid-state devices such as solid oxide fuel cells (SOFCs) and sensors. As the surface compositions of perovskites can greatly influence the catalytic properties, knowing and controlling their surface compositions is crucial to enhance device performance. In this study, we demonstrate that the surface strontium (Sr) and cobalt (Co) concentrations of perovskite-based thin films can be controlled reversibly at elevated temperatures by applying small electrical potential biases. The surface compositional changes of La 0.8Sr 0.2CoO 3-δ (LSC 113), (La 0.5Sr 0.5) 2CoO 4±δ (LSC 214), and LSC 214-decorated LSC 113 films (LSC 113/214) were investigated in situ by utilizing synchrotron-based X-ray photoelectron spectroscopy (XPS), where the largest changes of surface Sr were found for the LSC 113/214 surface. These findings offer the potential of reversibly controlling the surface functionality of perovskites. © 2011 American Chemical Society.

  1. Colonization of Bacteria on the Surfaces of Cold-Sprayed Copper Coatings Alters Their Electrochemical Behaviors

    Science.gov (United States)

    Suo, Xinkun; Abdoli, Leila; Liu, Yi; Xia, Peng; Yang, Guanjun; Li, Hua

    2017-04-01

    Copper coatings were fabricated on stainless steel plates by cold spraying. Attachment and colonization of Bacillus sp. on their surfaces in artificial seawater were characterized, and their effects on anticorrosion performances of the coatings were examined. Attached bacteria were observed using field emission scanning electron microscopy. Electrochemical behaviors including potentiodynamic polarization and electrochemical impedance spectroscopy with/without bacterial attachment were evaluated using commercial electrochemical analysis station Modulab. Results show that Bacillus sp. opt to settle on low-lying spots of the coating surfaces in early stage, followed by recruitment and attachment of extracellular polymeric substances (EPS) secreted through metabolism of Bacillus sp. The bacteria survive with the protection of EPS. An attachment model is proposed to illustrate the bacterial behaviors on the surfaces of the coatings. Electrochemical data show that current density under Bacillus sp. environment decreases compared to that without the bacteria. Charge-transfer resistance increases markedly in bacteria-containing seawater, suggesting that corrosion resistance increases and corrosion rate decreases. The influencing mechanism of bacteria settlement on corrosion resistance of the cold-sprayed copper coatings was discussed and elucidated.

  2. Electrochemical surface reshaping of polycrystalline platinum: Morphology and crystallography

    Energy Technology Data Exchange (ETDEWEB)

    Wei, X.; Reiner, A. [Electrochemistry Laboratory, Paul Scherrer Institut, CH-5232 Villigen PSI (Switzerland); Mueller, E. [Electron Microscopy ETH-Zuerich, CH-8093, Zuerich (Switzerland); Wokaun, A. [Electrochemistry Laboratory, Paul Scherrer Institut, CH-5232 Villigen PSI (Switzerland); Scherer, G.G. [Electrochemistry Laboratory, Paul Scherrer Institut, CH-5232 Villigen PSI (Switzerland)], E-mail: guenther.scherer@psi.ch; Zhang, L.; Shou, K.-Y.; Nelson, B.J. [Institute of Robotics and Intelligent Systems, ETH-Zuerich, CH-8092 Zuerich (Switzerland)

    2008-04-20

    A novel process of morphological evolution was observed on a polycrystalline platinum electrode surface during intensive potential perturbation in sulfuric acid electrolyte. The process was started from a smooth polycrystalline platinum surface, and ended up with a roughened overlayer which is composed of numerous morphological units. According to its appearance, the unit is named 'feather-like morphology (FLM)' which contains finer structures at nanometer scale. The active surface area of platinum at different stages during the morphological evolution was estimated by cyclic voltammetry. Electron microscopic measurements provided both morphological details and crystallographic information.

  3. Silicon surface biofunctionalization with dopaminergic tetrahydroisoquinoline derivatives

    Energy Technology Data Exchange (ETDEWEB)

    Lucena-Serrano, A.; Lucena-Serrano, C.; Contreras-Cáceres, R.; Díaz, A.; Valpuesta, M. [Dep. Química Orgánica, Facultad de Ciencias, Universidad de Málaga, 29071 Málaga (Spain); Cai, C. [Dep. Chemistry, University of Houston, Houston, TX 77204-5003 (United States); López-Romero, J.M., E-mail: jmromero@uma.es [Dep. Química Orgánica, Facultad de Ciencias, Universidad de Málaga, 29071 Málaga (Spain)

    2016-01-01

    Graphical abstract: - Highlights: • Two dopaminergic tetrahydroisoquinolines (THI) were synthesized. • Vinyl-terminated THI incorporated onto the H−Si(1 1 1) substrates via a hydrosilylation. • The highest yield in coverage was obtained in DMSO, at 4 h of irradiation and 0.1 mbar of vacuum. • Alkynyl-terminated Si surface was produced for incorporation of azide-THI by click reaction. • Best yields on grafted molecule were obtained by click reaction in absence of ascorbic acid. - Abstract: In this work we grafted vinyl- and azido-terminated tetrahydroisoquinolines (compounds 1 and 2, respectively) onto H−Si(1 1 1) silicon wafers obtaining highly stable modified surfaces. A double bond was incorporated into the tetrahydroisoquinoline structure of 1 to be immobilized by a light induced hydrosilylation reaction on hydrogen-terminated Si(1 1 1). The best results were obtained employing a polar solvent (DMSO), rather than a non-polar solvent (toluene). The azide derivative 2 was grafted onto alkenyl-terminated silicon substrates with copper-catalyzed azide-alkyne cycloaddition (CuAAC). Atomic force microscopy (AFM), contact angle goniometry (CA) and X-ray photoemission spectroscopy (XPS) were used to demonstrate the incorporation of 1 and 2 into the surfaces, study the morphology of the modified surfaces and to calculate the yield of grafting and surface coverage. CA measurements showed the increase in the surface hydrophobicity when 1 or 2 were incorporated into the surface. Moreover, compounds 1 and 2 were prepared starting from 1-(p-nitrophenyl)tetrahydroisoquinoline 3 under smooth conditions and in good yields. The structures of 1 and 2 were designed with a reduced A-ring, two substituents at positions C-6 and C-7, an N-methyl group and a phenyl moiety at C-1 in order to provide a high affinity against dopaminergic receptors. Moreover, O-demethylation of 1 was carried out once it was adsorbed onto the surface by treatment with BBr{sub 3}. The method

  4. Calibration of Electrochemical Capacitance-voltage Method on Pyramid Texture Surface Using Scanning Electron Microscopy

    Energy Technology Data Exchange (ETDEWEB)

    Komatsu, Y.; Cesar, I. [ECN Solar Energy, P.O.Box 1, 1755ZG Petten (Netherlands); Harata, D. [Department of Electronic Science and Engineering, Kyoto University, Nishikyo-ku, Kyoto 615-8530 (Japan); Schuring, E.W. [ECN Environment and Energy Engineering, P.O.Box 1, 1755ZG Petten (Netherlands); Vlooswijk, A.H.G.; Venema, P.R. [Tempress Systems BV, Radeweg 31, 8171MD Vaassen (Netherlands); Katori, S.; Fujita, S. [Photonics and Electronics Science and Engineering Center, Kyoto University, Nishikyo-ku, Kyoto 615-8530 (Japan)

    2013-07-01

    The electrochemical capacitance-voltage (ECV) technique can practically profile carrier concentrations on textured surfaces, but reliable calibration of the surface area is strongly demanded since it plays a decisive role in calculating both the carrier concentration and the profiling depth. In this work, we calibrate the area factor of pyramidally textured surfaces by comparing ECV profiles with cross-sectional scanning electron microscopy image, and found out it is 1.66, and not 1.73 which was formerly assumed. Furthermore, the calibrated area factor was applied to POCl3 and BBr3 diffusions which resulted in comparable diffusion profiles for both textured and polished surfaces.

  5. Electrochemical chlorine evolution at rutile oxide (110) surfaces

    DEFF Research Database (Denmark)

    Hansen, Heine Anton; Man, Isabela Costinela; Studt, Felix

    2010-01-01

    the lowest overpotential at which all elementary reaction steps in the chlorine evolution reaction are downhill in free energy. This condition is then used as a measure for catalytic activity. Linear scaling relations between the binding energies of the intermediates and the oxygen binding energies at cus......-sites are established for MO2 (M being Ir, Ru, Pt, Ti). The linear relations form the basis for constructing a generalized surface phase diagram where two parameters, the potential and the binding energy of oxygen, are needed to determine the surface composition. We calculate the catalytic activity as function...

  6. Surface Properties of PAN-based Carbon Fibers Modified by Electrochemical Oxidization in Organic Electrolyte Systems

    Directory of Open Access Journals (Sweden)

    WU Bo

    2016-09-01

    Full Text Available PAN-based carbon fibers were modified by electrochemical oxidization using fatty alcohol polyoxyethylene ether phosphate (O3P, triethanolamine (TEOA and fatty alcohol polyoxyethylene ether ammonium phosphate (O3PNH4 as organic electrolyte respectively. Titration analysis, single fiber fracture strength measurement and field emission scanning electron microscopy (FE-SEM were used to evaluate the content of acidic functional group on the surface, mechanical properties and surface morphology of carbon fiber. The optimum process of electrochemical treatment obtained is at 50℃ for 2min and O3PNH4 (5%, mass fraction as the electrolyte with current density of 2A/g. In addition, the surface properties of modified carbon fibers were characterized by X-ray photoelectron spectroscopy (XPS and single fiber contact angle test. The results show that the hydrophilic acidic functional groups on the surface of carbon fiber which can enhance the surface energy are increased by the electrochemical oxidation using O3PNH4 as electrolyte, almost without any weakening to the mechanical properties of carbon fiber.

  7. Electrochemical and surface characterization of a nickel-titanium alloy

    NARCIS (Netherlands)

    Wever, Dirk; Veldhuizen, AG; de Vries, J; Busscher, HJ; Uges, DRA; van Horn, James

    1998-01-01

    For clinical implantation purposes of shape memory metals the nearly equiatomic nickel-titanium (NiTi) alloy is generally used. In this study, the corrosion properties and surface characteristics of this alloy were investigated and compared with two reference controls, AISI 316 LVM stainless steel

  8. Evaluation of carbon nanotube fiber microelectrodes for neurotransmitter detection: Correlation of electrochemical performance and surface properties.

    Science.gov (United States)

    Yang, Cheng; Trikantzopoulos, Elefterios; Jacobs, Christopher B; Venton, B Jill

    2017-05-01

    Fibers made of CNTs are attractive microelectrode sensors because they can be directly fabricated into microelectrodes. Different protocols for making CNT fibers have been developed, but differences in surface structure and therefore electrochemical properties that result have not been studied. In this study, we correlated the surface and electrochemical properties for neurochemical detection at 3 types of materials: CNT fibers produced by wet spinning with (1) polyethylenimine (PEI/CNT) or (2) chlorosulfonic acid (CA/CNT), and (3) CNT yarns made by solid-based CNT drawing. CNT yarns had well-aligned, high purity CNTs, abundant oxygen functional groups, and moderate surface roughness which led to the highest dopamine current density (290 ± 65 pA/cm(2)) and fastest electron transfer kinetics. The crevices of the CNT yarn and PEI/CNT fiber microelectrodes allow dopamine to be momentarily trapped during fast-scan cyclic voltammetry detection, leading to thin-layer cell conditions and a response that was independent of applied waveform frequency. The larger crevices on the PEI/CNT fibers led to a slower time response, showing too much roughness is detrimental to fast detection. CA/CNT fibers have a smoother surface and lower currents, but their negative surface charge results in high selectivity for dopamine over uric acid or ascorbic acid. Overall, small crevices, high conductivity, and abundant oxygen groups led to high sensitivity for amine neurotransmitters, such as dopamine and serotonin. Thus, different surfaces of CNT fibers result in altered electrochemical properties and could be used in the future to predict and control electrochemical performance. Copyright © 2017 Elsevier B.V. All rights reserved.

  9. Surface Modification of MXenes: A Pathway to Improve MXene Electrode Performance in Electrochemical Energy Storage Devices

    KAUST Repository

    Ahmed, Bilal

    2017-12-31

    The recent discovery of layered transition metal carbides (MXenes) is one of the most important developments in two-dimensional (2D) materials. Preliminary theoretical and experimental studies suggest a wide range of potential applications for MXenes. The MXenes are prepared by chemically etching ‘A’-layer element from layered ternary metal carbides, nitrides and carbonitrides (MAX phases) through aqueous acid treatment, which results in various surface terminations such as hydroxyl, oxygen or fluorine. It has been found that surface terminations play a critical role in defining MXene properties and affects MXene performance in different applications such as electrochemical energy storage, electromagnetic interference shielding, water purification, sensors and catalysis. Also, the electronic, thermoelectric, structural, plasmonic and optical properties of MXenes largely depend upon surface terminations. Thus, controlling the surface chemistry if MXenes can be an efficient way to improve their properties. This research mainly aims to perform surface modifications of two commonly studied MXenes; Ti2C and Ti3C2, via chemical, thermal or physical processes to enhance electrochemical energy storage properties. The as-prepared and surface modified MXenes have been studied as electrode materials in Li-ion batteries (LIBs) and supercapacitors (SCs). In pursuit of desirable MXene surface, we have developed an in-situ room temperature oxidation process, which resulted in TiO2/MXene nanocomposite and enhanced Li-ion storage. The idea of making metal oxide and MXene nanocomposites was taken to the next level by combining a high capacity anode materials – SnO2 – and MXene. By taking advantage of already existing surface functional groups (–OH), we have developed a composite of SnO2/MXene by atomic layer deposition (ALD) which showed enhanced capacity and excellent cyclic stability. Thermal annealing of MXene at elevated temperature under different atmospheres was

  10. Potent 5-nitrofuran derivatives inhibitors of Trypanosoma cruzi growth: Electrochemical, spectroscopic and biological studies

    Science.gov (United States)

    Maria Aravena, C.; Claudio Olea, A.; Cerecetto, Hugo; González, Mercedes; Maya, Juan Diego; Rodríguez-Becerra, Jorge

    2011-07-01

    Cyclic voltammetry and electron spin resonance techniques were used in the investigation of several potential antiprotozoal containing thiosemicarbazone and carbamate nitrofurans. In the electrochemical behaviour, a self-protonation process involving the nitro group was observed. The reactivity of the nitro anion radical for these derivatives with glutathione, a biological relevant thiol, was also studied in means of cyclic voltammetry. These studies demonstrated that glutathione could react with radical species from 5-nitrofuryl system. Furthermore, from the voltammetric results, some parameters of biological significance as E71 (indicative of the biological nitro anion radical formation), and K (thermodynamic indicator the of oxygen redox cycling) have been calculated. We also evaluated the stability of the nitro anion radical in terms of the dimerization constant ( kd). The nitrofuran-free radicals from cyclic voltammetry were characterized by electron spin resonance. A clear dependence between both the thiosemicarbazone or carbamate substructure and the length of the linker, furyl- or furylpropenyl-spacer, and the delocalization of the unpaired electron was observed. Through of biological assays we obtained important parameters that account for the selective anti-trypanosomal activity of these derivatives. The trypomastigote viability study showed that all derivatives are as active as in the epimastigote form of the parasite in a doses dependent manner.

  11. Synthesis of surface roughed Pt nanowires and their application as electrochemical sensors for hydrogen peroxide detection.

    Science.gov (United States)

    Gao, Fan; Li, Zhiyang; Ruan, Dajiang; Gu, Zhiyong

    2014-09-01

    In this paper, platinum nanowires with roughed surface textures were fabricated by a galvanostatic electrodeposition method for electrochemical sensors toward hydrogen peroxide detection. The electrochemical behavior of the glassy carbon electrode modified with these nanowires has been studied for oxidation of hydrogen peroxide by using cyclic voltammetry and amperometry in phosphate buffer solution. Surface roughness was found to enhance the sensitivity of the Pt nanowire based electrochemical sensor towards H2O2. The Pt nanowires with rough surfaces displayed higher electrocatalytic response compared to nanowires with smooth surfaces, with a sensitivity of 171 μA mM(-1) cm(-2), and linear dynamic range up to 35 mM. The nanowire concentration effect on the sensing behavior was investigated with the best sensitivity output found at a nanowire concentration of roughly 8.6 x 10(7) number of nanowires/cm2. The new sensor also showed good anti-interference property and exhibited high accuracy when a real water sample containing H2O2 was measured.

  12. Imaging by Electrochemical Scanning Tunneling Microscopy and Deconvolution Resolving More Details of Surfaces Nanomorphology

    DEFF Research Database (Denmark)

    Andersen, Jens Enevold Thaulov

    to crystallographic-surface structures. Within the wide range of new technologies, those images surface features, the electrochemical scanning tunneling microscope (ESTM) provides means of atomic resolution where the tip participates actively in the process of imaging. Two metallic surfaces influence ions trapped.......g., nanoelectronics and single-molecule probing. In principle, the ESTM is capable of sub-atomic resolution but many details at this level of magnification need further treatment of recorded data before real information is obtained. Deconvolution of the data according to the instrument response may explain some...

  13. Study on micro fabricated stainless steel surface to anti-biofouling using electrochemical fabrication

    Science.gov (United States)

    Hwang, Byeong Jun; Lee, Sung Ho

    2017-12-01

    Biofilm formed on the surface of the object by the microorganism resulting in fouling organisms. This has led to many problems in daily life, medicine, health and industrial community. In this study, we tried to prevent biofilm formation on the stainless steel (SS304) sheet surface with micro fabricated structure. After then forming the microscale colloid patterns on the surface of stainless steel by using an electrochemical etching forming a pattern by using a FeCl3 etching was further increase the surface roughness. Culturing the Pseudomonas aeruginosa on the stainless steel fabricated with a micro structure on the surface was observed a relationship between the surface roughness and the biological fouling of the micro structure. As a result, the stainless steel surface with a micro structure was confirmed to be the biological fouling occurs less. We expect to be able to solve the problems caused by biological fouling in various fields such as medicine, engineering, using this research.

  14. Electrochemical CO2 reduction on Cu2O-derived copper nanoparticles: Controlling the catalytic selectivity of hydrocarbons

    NARCIS (Netherlands)

    Kas, Recep; Kortlever, R.; Milbrat, Alexander; Koper, M.T.M.; Mul, Guido; Baltrusaitis, Jonas

    2014-01-01

    The catalytic activity and hydrocarbon selectivity in electrochemical carbon dioxide (CO2) reduction on cuprous oxide (Cu2O) derived copper nanoparticles is discussed. Cuprous oxide films with [100], [110] and [111] orientation and variable thickness were electrodeposited by reduction of copper(II)

  15. Disposable screen printed graphite electrode for the direct electrochemical determination of ibuprofen in surface water

    KAUST Repository

    Amin, Sidra

    2014-08-01

    The potential of square wave voltammetry (SWV) for the determination of ibuprofen in aqueous solution, applying baseline correction, is reported. A screen printed graphite electrodes (SPGEs), especially pretreated for this purpose, were used to investigate the electrochemical oxidation and detection of ibuprofen. After optimization of SWV parameters, measurements were carried out at 200 Hz modulation frequency, 4 mV step potential and 40 mV pulse amplitude for the determination of ibuprofen. The surfaces of both untreated and pretreated SPGEs were characterized by scanning electron microscopy (SEM) and electrochemical impedance spectroscopy (EIS). The electro-catalytic properties of both the electrodes were correlated with the surface treatment. The pretreated screen printed graphite electrode exhibited a high sensitivity toward ibuprofen even in low concentration. The developed method was found rapid, cost-effective and reproducible for in-field ibuprofen detection.

  16. Ethylenediamine-modified oriented MCM-41 at the electrode surface, cobalt adsorption ability and electrochemical performance.

    Science.gov (United States)

    Rafiee, Mohammad; Karimi, Babak; Arshi, Simin; Vali, Hojatollah

    2014-03-28

    Mesoporous silica thin films (MCM-41) functionalized with ethylenediamine groups were electrochemically fabricated on electrode surfaces. These ligand functionalized film were a promising matrix for the immobilization of cobalt ions and preparation of cobalt complexes covalently bound to the MCM-41 support. The constructed MCM-41 were characterized by TEM, EDS and TGA analysis. This method yields uniform thin films with hexagonal mesochannels aligned and accessible to electrode surface. Well-defined electrode responses were, therefore, observed for the anchored complexes which made the electrochemical analysis of the structure possible as well. Voltammetric studies revealed the reactivity of the covalently bound complexes differed significantly from the dissolved ones. The anchored complexes preferred to be in their oxidized form which inhibits formation of oxygen adducts. The covalently bound complexes had relatively good leaching stability with good catalytic performance towards hydrogen peroxide reduction.

  17. Dynamic Characterization of Dendrite Deposition and Growth in Li-Surface by Electrochemical Impedance Spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Hernandez-Maya, R; Rosas, O; Saunders, J; Castaneda, H

    2015-01-13

    The evolution of dendrite formation is characterized by DC and AC electrochemical techniques. Interfacial mechanisms for lithium deposition are described and quantified by electrochemical impedance spectroscopy (EIS) between a lithium electrode and a graphite electrode. The initiation and growth of dendrites in the lithium surface due to the cathodic polarization conditions following anodic dissolution emulate long term cycling process occurring in the lithium electrodes. The dendrite initiation at the lithium/organic electrolyte interface is proposed to be performed through a combination of layering and interfacial reactions during different cathodic conditions. The growth is proposed to be performed by surface geometrical deposition. In this work, we use EIS in galvanostatic mode to assess the initiation and growth stages of dendrites by the accumulation of precipitates formed under different current conditions. The lithium/organic solvent experimental system using frequency domain techniques is validated by the theoretical approach using a deterministic model that accounts for the faradaic processes at the interface assuming a coverage fraction of the electrodic surface affected by the dendritic growth. (C) 2015 The Electrochemical Society. All rights reserved.

  18. Evaluating surface protonic transport on cerium oxide via electrochemical impedance spectroscopy measurement

    Science.gov (United States)

    Manabe, Ryo; Stub, Sindre Østby; Norby, Truls; Sekine, Yasushi

    2018-02-01

    Surface protonic transport on cerium oxide (CeO2) was investigated using electrochemical impedance spectroscopy (EIS). CeO2 pellets showing low relative density: approximately 60%, was prepared for the purpose. The structure and morphology of the prepared CeO2 pellets were confirmed from XRD and SEM measurements. Results show that the pellets had a pure cubic phase, with open pores on which water can be adsorbed. Electrochemical impedance spectroscopy measurements were taken to evaluate the surface protonic transport on CeO2 as a function of temperature and as a function of partial pressure of water (PH2O) at 400 °C. Investigations of the temperature dependence of the conductivity revealed that only the conductivities of surface grain bulk (σintra) and surface grain boundary (σinter) increased with decreasing temperatures under wet conditions (PH2O = 0.026 atm). The PH2O dependence of surface conductivities (σintra and σinter) revealed that σintra increases strongly with PH2O at 400 °C. These findings provide evidence that water adsorbates play an important role in surface protonic transport on CeO2 at low temperatures. Surface protonic transport at low temperatures can contribute to the expansion of applications for electrical and catalytic processes.

  19. Measurement of the specific surface area of loose copper deposit by electrochemical methods

    Directory of Open Access Journals (Sweden)

    E. A. Dolmatova

    2016-07-01

    Full Text Available In the work the surface area of the electrode with dispersed copper deposit obtained within 30 seconds was evaluated by techniques of chronopotentiometry (CPM and impedance spectroscopy. In method CPM the electrode surface available for measurement depends on the value of the polarizing current. At high currents during the transition time there is a change of surface relief that can not determine the full surface of loose deposit. The electrochemical impedance method is devoid of this shortcoming since the measurements are carried out in indifferent electrolyte in the absence of current. The area measured by the impedance is tens of times higher than the value obtained by chronopotentiometry. It is found that from a solution containing sulfuric acid the deposits form with a high specific surface area. Based on these data it was concluded that the method of impedance spectroscopy can be used to measure in situ the surface area of the dispersed copper deposits.

  20. Surface-treated commercially pure titanium for biomedical applications: Electrochemical, structural, mechanical and chemical characterizations

    Energy Technology Data Exchange (ETDEWEB)

    Ogawa, Erika S.; Matos, Adaias O.; 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); 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); Sukotjo, Cortino [Department of Restorative Dentistry, University of Illinois at Chicago, College of Dentistry, 801 S Paulina, Chicago, IL, USA, 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 Biomedical Sciences, University of Illinois, College of Medicine at Rockford, 1601 Parkview Avenue, Rockford, IL, USA, 61107 (United States); Rangel, Elidiane C.; Cruz, Nilson C. [IBTN/Br—Institute of Biomaterials, Tribocorrosion and Nanomedicine—Brazilian Branch (Brazil); Laboratory of Technological Plasmas, Engineering College, Univ Estadual Paulista (UNESP), Av Três de Março, 511, Sorocaba, São Paulo 18087-180 (Brazil); Mesquita, Marcelo F.; Consani, Rafael X. [Department of Prosthodontics and Periodontology, Piracicaba Dental School, University of Campinas (UNICAMP), Av Limeira, 901, Piracicaba, São Paulo 13414-903 (Brazil); and others

    2016-08-01

    Modified surfaces have improved the biological performance and biomechanical fixation of dental implants compared to machined (polished) surfaces. However, there is a lack of knowledge about the surface properties of titanium (Ti) as a function of different surface treatment. This study investigated the role of surface treatments on the electrochemical, structural, mechanical and chemical properties of commercial pure titanium (cp-Ti) under different electrolytes. Cp-Ti discs were divided into 6 groups (n = 5): machined (M—control); etched with HCl + H{sub 2}O{sub 2} (Cl), H{sub 2}SO{sub 4} + H{sub 2}O{sub 2} (S); sandblasted with Al{sub 2}O{sub 3} (Sb), Al{sub 2}O{sub 3} followed by HCl + H{sub 2}O{sub 2} (SbCl), and Al{sub 2}O{sub 3} followed by H{sub 2}SO{sub 4} + H{sub 2}O{sub 2} (SbS). Electrochemical tests were conducted in artificial saliva (pHs 3; 6.5 and 9) and simulated body fluid (SBF—pH 7.4). All surfaces were characterized before and after corrosion tests using atomic force microscopy, scanning electron microscopy, energy dispersive microscopy, X-ray diffraction, surface roughness, Vickers microhardness and surface free energy. The results indicated that Cl group exhibited the highest polarization resistance (R{sub p}) and the lowest capacitance (Q) and corrosion current density (I{sub corr}) values. Reduced corrosion stability was noted for the sandblasted groups. Acidic artificial saliva decreased the R{sub p} values of cp-Ti surfaces and produced the highest I{sub corr} values. Also, the surface treatment and corrosion process influenced the surface roughness, Vickers microhardness and surface free energy. Based on these results, it can be concluded that acid-etching treatment improved the electrochemical stability of cp-Ti and all treated surfaces behaved negatively in acidic artificial saliva. - Highlights: • Characterization of surface treatment for biomedical implants was investigated. • Sandblasting reduced the corrosion stability of cp

  1. Probing surface and bulk electrochemical processes on the LaAlO3-SrTiO3 interface

    Energy Technology Data Exchange (ETDEWEB)

    Kumar, Amit [ORNL; Arruda, Thomas M [ORNL; Kim, Yunseok [ORNL; Ivanov, Ilia N [ORNL; Jesse, Stephen [ORNL; Bark, C [University of Wisconsin, Madison; Bristowe, Nicholas C [University of Cambridge; Artacho, Emilio [University of Cambridge; Littlewood, Peter B [ORNL; Eom, Professor Chang-Beom [University of Wisconsin, Madison; Kalinin, Sergei V [ORNL

    2012-01-01

    Local electrochemical phenomena on the surfaces of LaAlO3-SrTiO3 heterostructure are explored using unipolar and bipolar dynamic electrochemical strain microscopy (D-ESM). The D-ESM suggests the presence of at least two distinct electrochemical processes, including fast reversible low-voltage process and slow high-voltage process. The latter process is associated with static surface deformations in the sub-nm regime. These behaviors are compared with Kelvin Probe Force Microscopy hysteresis data. The possible origins of observed phenomena are discussed and these studies suggest that charge-writing behavior in LAO-STO include strong surface/bulk electrochemical component and are more complicated than simple screening by surface adsorbates.

  2. Probing surface and bulk electrochemical processes on the LaAlO3-SrTiO3 interface.

    Science.gov (United States)

    Kumar, Amit; Arruda, Thomas M; Kim, Yunseok; Ivanov, Ilia N; Jesse, Stephen; Bark, Chung W; Bristowe, Nicholas C; Artacho, Emilio; Littlewood, Peter B; Eom, Chang-Beom; Kalinin, Sergei V

    2012-05-22

    Local electrochemical phenomena on the surfaces of the LaAlO(3)-SrTiO(3) heterostructure are explored using unipolar and bipolar dynamic electrochemical strain microscopy (D-ESM). The D-ESM suggests the presence of at least two distinct electrochemical processes, including fast reversible low-voltage process and slow high-voltage process. The latter process is associated with static surface deformations in the sub-nanometer regime. These behaviors are compared with Kelvin probe force microscopy hysteresis data. The possible origins of observed phenomena are discussed, and these studies suggest that charge-writing behavior in LAO-STO includes a strong surface/bulk electrochemical component and is more complicated than simple screening by surface adsorbates.

  3. A novel electrochemical method to detect cell surface carbohydrates and target cells.

    Science.gov (United States)

    Shao, Zhenyu; Li, Yun; Yang, Qianlu; Wang, Jing; Li, Genxi

    2010-12-01

    Glycosylation of cell surfaces is a critical factor in many biological processes; however, the lack of effective analytical tools for the detection of cell surface carbohydrates has been the bottleneck for probing into the processes. In this paper, a novel electrochemical method is presented for the analysis of cell surface carbohydrates, which can be also used to detect the target cells. Firstly, 5-hydroxy-3-hexanedithiol-1,4-naphthoquinone (JUG(thio)), the electrochemical reporter, and anti-selectin aptamer are successively modified onto the surface of a gold electrode. Different concentrations of intestinal human colon adenocarcinoma (LS180) cells are employed as the target cells for this study. Consequently, the specific carbohydrates on the surfaces of LS180 cells and anti-selectin aptamers will compete for combination with selectin in the system. As a result, the oxidation signal of JUG(thio) is changed and the detection of the cell surface carbohydrates can be achieved easily and sensitively. Furthermore, the proposed method can be used to specifically detect LS180 cells in a wide concentration range, from 10(3) to 10(7) cells/mL, with a good linear relationship and low detection limit, which might be promising for the diagnosis of cancer and some other diseases in the future.

  4. In situ AFM investigation of electrochemically induced surface-initiated atom-transfer radical polymerization.

    Science.gov (United States)

    Li, Bin; Yu, Bo; Zhou, Feng

    2013-02-12

    Electrochemically induced surface-initiated atom-transfer radical polymerization is traced by in situ AFM technology for the first time, which allows visualization of the polymer growth process. It affords a fundamental insight into the surface morphology and growth mechanism simultaneously. Using this technique, the polymerization kinetics of two model monomers were studied, namely the anionic 3-sulfopropyl methacrylate potassium salt (SPMA) and the cationic 2-(metharyloyloxy)ethyltrimethylammonium chloride (METAC). The growth of METAC is significantly improved by screening the ammonium cations by the addition of ionic liquid electrolyte in aqueous solution. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  5. An Overview on Recent Progress in Electrochemical Biosensors for Antimicrobial Drug Residues in Animal-Derived Food

    Science.gov (United States)

    Majdinasab, Marjan; Yaqub, Mustansara; Rahim, Abdur; Catanante, Gaelle; Hayat, Akhtar; Marty, Jean Louis

    2017-01-01

    Anti-microbial drugs are widely employed for the treatment and cure of diseases in animals, promotion of animal growth, and feed efficiency. However, the scientific literature has indicated the possible presence of antimicrobial drug residues in animal-derived food, making it one of the key public concerns for food safety. Therefore, it is highly desirable to design fast and accurate methodologies to monitor antimicrobial drug residues in animal-derived food. Legislation is in place in many countries to ensure antimicrobial drug residue quantities are less than the maximum residue limits (MRL) defined on the basis of food safety. In this context, the recent years have witnessed a special interest in the field of electrochemical biosensors for food safety, based on their unique analytical features. This review article is focused on the recent progress in the domain of electrochemical biosensors to monitor antimicrobial drug residues in animal-derived food. PMID:28837093

  6. Facile Electrochemical Method to Improve Surface Features of Pure Copper in Dilute Basic Solutions

    Science.gov (United States)

    Fattah-alhosseini, Arash; Imantalab, Omid; Attarzadeh, Farid Reza; Attarzadeh, Navid

    2017-04-01

    Electrochemical properties of coarse and nano-grained pure copper can be modified and improved effectively through applying cyclic potentiodynamic passivation (CPP) treatment. It is found that the success of this method depends up to a large extent on grain size. Eight passes of accumulative roll bonding processing are successfully used at room temperature to produce nano-grained pure copper. Transmission electron microscopy image and selected area diffraction pattern both attest to the occurrence of intense grain refinement under the influence of aforementioned process, in which an average grain size <100 nm is attainable. Using several electrochemical characterization methods reveals that CPP treatment fully exploits potentials of nano-grained samples to form a dense and thick protective passive film. It is speculated that high-quality passive layers relate to the presence of high-density structural defects on the surface of nano-grained samples.

  7. Mechanistic study of in vitro chemical interaction of trimipramine drug with barbituric derivative after its oxidation: Electrochemical synthesis of new dibenzazepine derivative.

    Science.gov (United States)

    Lotfi, Shahram; Tammari, Esmail; Nezhadali, Azizollah

    2017-07-01

    Electrochemical oxidation of trimipramine in the absence and presence of 1,3 dimethyl barbituric acid as a nucleophile in aqueous solution has been studied using cyclic voltammetry and controlled-potential coulometry electrolysis. Voltammetric studies of electro-oxidation of trimipramine were realized in a range of pH1.0 to 8.0 in the absence and presence of 1,3 dimethyl barbituric acid. Based on the obtained electrochemical results, dimerization is the main reaction of electro-oxidation of trimipramine in the absence of nucleophile. The voltammetric data indicate that the 1,3 dimethyl barbituric acid participation in Michael addition reaction with the oxidized dimeric form of trimipramine via an ECEC electrochemical mechanisms. On the other hand the results indicate existence of a catalytic (EC') electrochemical mechanism in parallel with ECEC electrochemical mechanism. This method provides a facile and one-pot procedure for the synthesis of new dibenzazepine derivative. Finally, a possible mechanism is proposed for the electrode process, on the basis of the present and previous investigations. The product has been characterized by IR, (1)H NMR, (13)CNMR and MS methods. Copyright © 2017. Published by Elsevier B.V.

  8. Electrochemical deposition and surface-initiated RAFT polymerization: protein and cell-resistant PPEGMEMA polymer brushes.

    Science.gov (United States)

    Tria, Maria Celeste R; Grande, Carlos David T; Ponnapati, Ramakrishna R; Advincula, Rigoberto C

    2010-12-13

    This paper introduces a novel and versatile method of grafting protein and cell-resistant poly(poly ethylene glycol methyl ether methacrylate) (PPEGMEMA) brushes on conducting Au surface. The process started with the electrochemical deposition and full characterization of an electro-active chain transfer agent (CTA) on the Au surface. The electrochemical behavior of the CTA was investigated by cyclic voltammetry (CV) while the deposition and stability of the CTA on the surface were confirmed by ellipsometry, contact angle, and X-ray photoelectron spectroscopy (XPS). The capability of the electrodeposited CTA to mediate surface-initiated reversible addition-fragmentation chain transfer (SI-RAFT) polymerization on both the polymethyl methacrylate (PMMA; model polymer) and PPEGMEMA brushes was demonstrated by the increase in thicknesses of the films after polymerization. Contact angles also decreased with the incorporation of the more hydrophilic brushes. Significant changes in the morphologies of the films before and after polymerization were also observed with atomic force microscopy (AFM) analyses. Furthermore, XPS results showed an increase in the O 1s peak intensity relative to C 1s after polymerizations, which confirmed the grafting of polyethyleneglycol (PEG) bearing brushes. The ability of the PPEGMEMA-modified Au surface to resist nonspecific adhesion of proteins and cells was monitored and confirmed by XPS, ellipsometry, contact angle, AFM, and fluorescence imaging. The new method presented has potential application as robust protein and cell-resistant coatings for electrically conducting electrodes and biomedical devices.

  9. Correlation of Spectral and Electrochemical Properties of a Series of Ferrocene Derivatives

    Science.gov (United States)

    Hepp, Aloysius F.; Wrighton, Mark S.

    2016-01-01

    Charge-transfer-to-solvent (CTTS) bands are observed in the UV/VIS spectra of a series of ferrocene derivatives (ferrocene; 1,1'-dimethyl; 1,2,3,4,5-pentamethyl; 1,2,3,4,l',2',3',4'-octamethyl; and decamethyl) by the addition of increasing amounts of CCl4 to ethanol solutions. A linear correlation (slope = 8540 cm-1/V) was found between the redox potential and the energy of the CTTS band, consistent with electrochemical and photochemical oxidation by removal of an electron from the same molecular orbital. Inclusion of literature data for ruthenocene and [(?5-C5H5)Fe(CO)]4 results in a line with a slope of 8140 cm-1/V, within 1 percent of the wavenumber to electron volt conversion factor. Calculation of association constants (K) shows a slight decrease (1.2 to 0.7 mole fraction-1) as the bulkiness of the cyclopentadienyl ring increases, consistent with either a steric or a repulsive electronic effect. The extinction coefficient of the CTTS absorption was constant at approximately 1700/M/cm.

  10. Derivation of finite element formulation for electrochemical governing equations of ionic polymer actuators

    Energy Technology Data Exchange (ETDEWEB)

    Kang, Sung Soo [Jeonju University, Jeonju (Korea, Republic of)

    2013-01-15

    Ionic polymer actuators have recently attracted a great deal of interest as electroactive materials with potentials as soft actuators, sensors, artificial muscles, robotics, and microelectromechanical systems because of their numerous advantages, including low voltage requirement, high compliance, lightness, and flexibility. The platinum-plated Nafion, a perfluorosulfonic acid membrane made by Dupont, is commonly used as a polyelectrolyte in actuator applications. The bending of the ionic polymer actuators in an electric field is dominated by the electro-osmosis of hydrated ions and slow diffusion of free water molecules. The changes in hydration cause a local volumetric strain resulting in bending deformation, such as expansion and contraction. In this study, a two-dimensional finite element (FE) formulation based on the Galerkin method is derived for the governing equations describing these electrochemical responses. In addition, a three-dimensional FE deformation analysis is conducted on the bending behaviors of the platinum-plated ionic polymer actuators. Several numerical studies for ionic polymer actuators, such as plates with various electrode arrangements and disk models in electric field, are performed to confirm the validity of the proposed formulation.

  11. Room-temperature Electrochemical Synthesis of Carbide-derived Carbons and Related Materials

    Energy Technology Data Exchange (ETDEWEB)

    Gogotsi, Yury [Drexel Univ., Philadelphia, PA (United States). Nanomaterials Group. Materials Science and Engineering Dept.

    2015-02-28

    This project addresses room-temperature electrochemical etching as an energy-efficient route to synthesis of 3D nanoporous carbon networks and layered 2D carbons and related structures, as well as provides fundamental understanding of structure and properties of materials produced by this method. Carbide-derived-carbons (CDCs) are a growing class of nanostructured carbon materials with properties that are desirable for many applications, such as electrical energy and gas storage. The structure of these functional materials is tunable by the choice of the starting carbide precursor, synthesis method, and process parameters. Moving from high-temperature synthesis of CDCs through vacuum decomposition above 1400°C and chlorination above 400°C, our studies under the previous DOE BES support led to identification of precursor materials and processing conditions for CDC synthesis at temperatures as low as 200°C, resulting in amorphous and highly reactive porous carbons. We also investigated synthesis of monolithic CDC films from carbide films at 250-1200°C. The results of our early studies provided new insights into CDC formation, led to development of materials for capacitive energy storage, and enabled fundamental understanding of the electrolyte ions confinement in nanoporous carbons.

  12. A new Co (III) complex of Schiff base derivative for electrochemical ...

    Indian Academy of Sciences (India)

    The complex has been combined with polyvinyl chloride (PVC) membrane of various compositions and tested as an electrochemical electrode towards recognition of several anions. The electrode exhibits exceptional electrochemical recognition for the nitrite (NO⁻ ₂ ) anion in aqueous media. The electrode exhibited a ...

  13. Non-machined Surface Protection Process of Electrochemical Machining Based on Repaired Turbine Blade

    Directory of Open Access Journals (Sweden)

    LIU Wei-dong

    2016-11-01

    Full Text Available In order to improve the efficiency of turbine blade repairing, protection processes of non-machined surface in Electrochemical Machining (ECM based on blade repairing were studied. Mathematical model of electric field was developed to obtain current density distribution on anode surface, and to study the repairing principle and consequently analyze the defects forming mechanism by conventional electrolytic repair process. Sacrificial layer process was proposed to protect the non-machined surface in this work and an experimental system was developed to shape overlay welded TC4 blades. The results show that directly shaping process and insulated layer process produce stray dissolution and "stair" defects respectively,while sacrificial layer process achieves acceptable machining performance. With shaping time of 60s, the efficiency is improved; shaped blades have higher precision and surface roughness is Ra≤0.6μm, and with higher repeatability, the design requirements can be met.

  14. Surface molecularly imprinted polymers-based electrochemical sensor for bovine hemoglobin recognition.

    Science.gov (United States)

    Li, Lu; Yang, Lingling; Xing, Zonglan; Lu, Xiaojing; Kan, Xianwen

    2013-11-21

    A novel electrochemical sensor for bovine hemoglobin (BHb) recognition and detection was prepared by a surface molecularly imprinted technique. Aldehyde group-functionalized silica microspheres were modified on an Au electrode surface, and these were subsequently covalently bound with the template molecule, BHb, through imine bonds. Electropolymerization was performed to deposit polypyrrole onto the above modified electrode surface. A three-dimensional macroporous structural sensor was obtained after etching of silica and the extraction of BHb. Differential pulse voltammetry (DPV) and electrochemical impedance spectroscopy (EIS) were employed to characterize the fabrication process of the sensor using [Fe(CN)6](3-)/[Fe(CN)6](4-) as an electroactive probe. Since all imprinted cavities were situated at the surface of the polymers, the prepared sensor exhibited considerably fast binding kinetics. Compared to other non-template proteins, the sensor showed an excellent recognition capacity for BHb. Moreover, the prepared sensor also exhibited a dependent relationship between the concentration of BHb and the peak current of [Fe(CN)6](3-)/[Fe(CN)6](4-).

  15. Electrochemical formation and characterization of Au nanostructures on a highly ordered pyrolytic graphite surface

    Energy Technology Data Exchange (ETDEWEB)

    Arroyo Gómez, José J. [Instituto de Ingeniería Electroquímica y Corrosión (INIEC ), Departamento de Ingeniería Química, Universidad Nacional del Sur, Avda. Alem 1253, 8000 Bahía Blanca (Argentina); Zubieta, Carolina; Ferullo, Ricardo M. [INQUISUR , Departamento de Química, Universidad Nacional del Sur, Avda. Alem 1253, 8000 Bahía Blanca (Argentina); García, Silvana G., E-mail: sgarcia@criba.edu.ar [Instituto de Ingeniería Electroquímica y Corrosión (INIEC ), Departamento de Ingeniería Química, Universidad Nacional del Sur, Avda. Alem 1253, 8000 Bahía Blanca (Argentina)

    2016-02-15

    Graphical abstract: - Highlights: • The electrodeposition of Au on HOPG tends to follow the response predicted for a 3D instantaneous nucleation mechanism in the potential range considered. • By choosing suitable nucleation and growth pulses, one-dimensional deposits were possible, preferentially located on step edges of the HOPG substrate. • Quantum-mechanical calculations confirmed the tendency of Au atoms to join selectively on the HOPG step edges, at the early stages of Au electrodeposition. - Abstract: The electrochemical formation of Au nanoparticles on a highly ordered pyrolytic graphite (HOPG) substrate using conventional electrochemical techniques and ex-situ AFM is reported. From the potentiostatic current transients studies, the Au electrodeposition process on HOPG surfaces was described, within the potential range considered, by a model involving instantaneous nucleation and diffusion controlled 3D growth, which was corroborated by the microscopic analysis. Initially, three-dimensional (3D) hemispherical nanoparticles distributed on surface defects (step edges) of the substrate were observed, with increasing particle size at more negative potentials. The double potential pulse technique allowed the formation of rounded deposits at low deposition potentials, which tend to form lines of nuclei aligned in defined directions leading to 3D ordered structures. By choosing suitable nucleation and growth pulses, one-dimensional (1D) deposits were possible, preferentially located on step edges of the HOPG substrate. Quantum-mechanical calculations confirmed the tendency of Au atoms to join selectively on surface defects, such as the HOPG step edges, at the early stages of Au electrodeposition.

  16. Electrochemical analysis of the UV treated bactericidal Ti6Al4V surfaces.

    Science.gov (United States)

    Pacha-Olivenza, Miguel A; Gallardo-Moreno, Amparo M; Vadillo-Rodríguez, Virginia; González-Martín, M Luisa; Pérez-Giraldo, Ciro; Galván, Juan C

    2013-04-01

    This research investigates in detail the bactericidal effect exhibited by the surface of the biomaterial Ti6Al4V after being subjected to UV-C light. It has been recently hypothesized that small surface currents, occurring as a consequence of the electron-hole pair recombination taking place after the excitation process, are behind the bactericidal properties displayed by this UV-treated material. To corroborate this hypothesis we have used different electrochemical techniques, such as electrochemical impedance spectroscopy (EIS), potentiodynamic polarization plots and Mott-Schottky plots. EIS and Mott-Schottky plots have shown that UV-C treatment causes an initial increase on the surface electrical conduction of this material. In addition, EIS and polarization plots demonstrated that higher corrosion currents occur at the UV treated than at the non-irradiated samples. Despite this increase in the corrosion currents, EIS has also shown that such currents are not likely to affect the good stability of this material oxide film since the irradiated samples completely recovered the control values after being stored in dark conditions for a period not longer than 24h. These results agree with the already-published in vitro transitory behavior of the bactericidal effect, which was shown to be present at initial times after the biomaterial implantation, a crucial moment to avoid a large number of biomaterial associated infections. Copyright © 2013 Elsevier B.V. All rights reserved.

  17. Droplet electrochemical study of the pH dependent redox behavior of novel ferrocenyl-carborane derivatives and its application in specific cancer cell recognition

    Energy Technology Data Exchange (ETDEWEB)

    Wu, Changyu [State Key Laboratory of Bioelectronics (Chien-Shiung Wu Laboratory), Southeast University, Nanjing 210096 (China); Shah, Afzal [Department of Chemistry, Quaid-i-Azam University, Islamabad 45320 (Pakistan); Ye, Hongde [State Key Laboratory of Coordination Chemistry, Nanjing University, Nanjing 210093 (China); Chen, Xiao; Ye, Jing; Jiang, Hui [State Key Laboratory of Bioelectronics (Chien-Shiung Wu Laboratory), Southeast University, Nanjing 210096 (China); Chen, Baoan [Department of Hematology, the Affiliated Zhongda Hospital, Clinical Medical School, Southeast University, Nanjing 210009 (China); Wang, Xuemei, E-mail: xuewang@seu.edu.cn [State Key Laboratory of Bioelectronics (Chien-Shiung Wu Laboratory), Southeast University, Nanjing 210096 (China); Yan, Hong, E-mail: hyan1965@nju.edu.cn [State Key Laboratory of Coordination Chemistry, Nanjing University, Nanjing 210093 (China)

    2015-02-01

    Highlights: • Electrochemical behaviors of novel ferrocenyl based carboranes (FcCB) were explored with a droplet system. • The shifts of peak potentials with changes of pH values indicated the involvement of proton during electron transfer reaction. • Normal cells and cancer cells could be specifically recognized by using FcCB as probe. • This electrochemical method in a droplet shows great potential application for relevant diagnostics of clinical samples. - Abstract: Novel ferrocenyl based carboranes (FcCBs) and their distinguish behavior for cancer cell recognition have been explored in this contribution. The voltammetric study in a droplet of 10 μL placed on the surface of a glassy carbon electrode demonstrates the excellent electrochemical behavior of FcCBs, which could be further exploited for establishing the promising and sensitive biosensors. The FcCBs’ redox behavior is examined in a wide pH range, and square wave voltammetry revealed the reversible and irreversible nature of first and second anodic peaks. The obvious shifts in peak potentials corresponding with the change of pH values demonstrate the abstraction of electrons to be accompanied with the transfer of protons. By using the droplet electrochemical technique, FcCBs can be employed to distinguish normal and cancer cells with a linear range from 1.0 × 10{sup 3} to 3.0 × 10{sup 4} cells mL{sup −1} and the limit of detection at 800 cells mL{sup −1}. The novel carborane derivatives could be utilized as important potential molecular probes for specific recognition of cancer cells like leukemia cells from normal cells.

  18. A study of electrodischarge machining–pulse electrochemical machining combined machining for holes with high surface quality on superalloy

    OpenAIRE

    Ning Ma; Xiaolong Yang; Mingqian Gao; Jinlong Song; Ganlin Liu; Wenji Xu

    2015-01-01

    Noncircular holes on the surface of turbine rotor blades are usually machined by electrodischarge machining. A recast layer containing numerous micropores and microcracks is easily generated during the electrodischarge machining process due to the rapid heating and cooling effects, which restrict the wide applications of noncircular holes in aerospace and aircraft industries. Owing to the outstanding advantages of pulse electrochemical machining, electrodischarge machining–pulse electrochemic...

  19. Electrochemical Characteristics of Titanium for Dental Implants in Case of the Electroless Surface Modification

    Directory of Open Access Journals (Sweden)

    Klimecka-Tatar D.

    2016-06-01

    Full Text Available In the paper the results of research under effect of electroless phosphate coating of titanium dental implants on potentiokinetic polarization characteristic obtained in artificial saliva were presented. On the basis of electrochemical studies it was concluded that the electroless process of phosphating beneficialy effect on corrosion characteristic of titanium determined in solution simulating the oral cavity. Furthermore, the proposed technique of chemical treatment of titanium surface is conducive to the homogeneous development of the surface, which is extremely important from the point of view of titanium implants biointegration. Phosphating treatment affect on the development of surface geometry, resulting in a slight increase in roughness parameters (Ra, Rz and Rmax. The temperature increase of electroless phosphating treatment promotes the rate of conversion layer formation, whereas the effect of temperature of the chemical treatment efficiency is secondary important at longer exposure times (e.g. 45 minutes.

  20. Porous carbon nanospheres derived from chlorination of bis(cyclopentadienyl)titanium dichloride and their electrochemical capacitor performance

    Energy Technology Data Exchange (ETDEWEB)

    Gonzalez-Garcia, Pedro, E-mail: pegonzal@quim.ucm.es [Departamento de Quimica Inorganica, Facultad de Ciencias Quimicas, Universidad Complutense, E-28040 Madrid (Spain); Centeno, T.A. [Instituto Nacional del Carbon-CSIC, Apartado 73, E-33080 Oviedo (Spain); Urones-Garrote, Esteban [Centro de Microscopia y Citometria, Universidad Complutense, E-28040 Madrid (Spain); Avila-Brande, David; Otero-Diaz, L. Carlos [Departamento de Quimica Inorganica, Facultad de Ciencias Quimicas, Universidad Complutense, E-28040 Madrid (Spain)

    2011-10-17

    Highlights: {yields} Microporous carbon nanospheres have been produced via chlorination reaction of bis(cyclopentadienyl)titanium dichloride. {yields} The materials present a structure formed by disordered arrangements of graphene-like layers, sp{sup 2}/sp{sup 3} ratio {approx}95-97% and mass-density below pure graphite. {yields} The increase in the reaction temperature decreases the particle size distribution and improves the surface area and the micropore volume. {yields} Electrochemical performance for the 900 deg. C sample shows a specific capacitance of 106 F g{sup -1} in H{sub 2}SO{sub 4} electrolyte and 80 F g{sup -1} in (C{sub 2}H{sub 5}){sub 4}NBF{sub 4}/acetonitrile medium. - Abstract: Conglomerated and accreted porous carbon spheres have been obtained by the chlorination reaction of bis(cyclopentadienyl)titanium dichloride as carbon precursor. The spheres size distribution, derived from scanning electron microscopy observations, shows that the diameter intervals decreases from 70-525 nm at 400 deg. C to 40-370 nm at 900 deg. C. High-resolution transmission electron microscopy observations indicate that the spheres are formed by open and curved randomly stacked graphene-like layers. Electron energy loss spectroscopy studies show relative sp{sup 2}/sp{sup 3} ratio higher than 95% and mass-density values (1.1-1.6 g cm{sup -3}) smaller than graphite. Nitrogen adsorption measurements reveal the presence of micro and mesopores whose contributions to the total porosity greatly depend on the preparation temperature. Galvanostatic charging-discharging measurements on the carbon material synthesized at 900 deg. C provide a specific capacitance of 106 F g{sup -1} in the aqueous H{sub 2}SO{sub 4} electrolyte and 80 F g{sup -1} in the aprotic (C{sub 2}H{sub 5}){sub 4}NBF{sub 4}/acetonitrile medium. These high values suggest the potentiality of this material for electrical energy storage in electrochemical double layer capacitors.

  1. Evapotranspiration Derived from Satellite Observed Surface Temperatures

    NARCIS (Netherlands)

    Klaassen, Wim; Berg, Wim van den

    1985-01-01

    Evapotranspiration is calculated from surface temperatures using an energy balance method. This method is sensitive to the temperature difference between the surface and the air above, and somewhat to the windspeed. In this study we consider the influence of the spatial variability of air

  2. A mathematical model for surface roughness of fluidic channels produced by grinding aided electrochemical discharge machining (G-ECDM

    Directory of Open Access Journals (Sweden)

    Ladeesh V. G.

    2017-01-01

    Full Text Available Grinding aided electrochemical discharge machining is a hybrid technique, which combines the grinding action of an abrasive tool and thermal effects of electrochemical discharges to remove material from the workpiece for producing complex contours. The present study focuses on developing fluidic channels on borosilicate glass using G-ECDM and attempts to develop a mathematical model for surface roughness of the machined channel. Preliminary experiments are conducted to study the effect of machining parameters on surface roughness. Voltage, duty factor, frequency and tool feed rate are identified as the significant factors for controlling surface roughness of the channels produced by G-ECDM. A mathematical model was developed for surface roughness by considering the grinding action and thermal effects of electrochemical discharges in material removal. Experiments are conducted to validate the model and the results obtained are in good agreement with that predicted by the model.

  3. Electrochemical Oxidative Decarboxylation of Malonic Acid Derivatives: A Method for the Synthesis of Ketals and Ketones.

    Science.gov (United States)

    Ma, Xiaofeng; Luo, Xiya; Dochain, Simon; Mathot, Charlotte; Markò, István E

    2015-10-02

    A novel electrochemical oxidative decarboxylation of disubstituted malonic acids leading to dimethoxy ketals is described. In the presence of NH3, a wide range of disubstituted malonic acids was transformed into the corresponding ketals in good to excellent yields under electrochemical conditions. When the crude reaction mixture, obtained after electrolysis, was directly treated with 1 M aq HCl, the initially generated ketals were smoothly transformed into the corresponding ketones in a single vessel operation.

  4. Surface properties of nanostructured NiO undergoing electrochemical oxidation in 3-methoxy-propionitrile

    Energy Technology Data Exchange (ETDEWEB)

    Bonomo, Matteo [Department of Chemistry, University of Rome “La Sapienza”, Piazzale Aldo Moro 5, 00185 Rome (Italy); Marrani, Andrea Giacomo, E-mail: andrea.marrani@uniroma1.it [Department of Chemistry, University of Rome “La Sapienza”, Piazzale Aldo Moro 5, 00185 Rome (Italy); Novelli, Vittoria [Department of Chemistry, University of Rome “La Sapienza”, Piazzale Aldo Moro 5, 00185 Rome (Italy); Awais, Muhammad [Department of Industrial Engineering, “King Abdulaziz” University, Rabigh (Saudi Arabia); Solar Energy Conversion Strategic Research Cluster, University College Dublin (UCD), Belfield, Dublin 4 (Ireland); Dowling, Denis P. [Solar Energy Conversion Strategic Research Cluster, University College Dublin (UCD), Belfield, Dublin 4 (Ireland); School of Mechanical and Materials Engineering, University College Dublin (UCD), Belfield, Dublin 4 (Ireland); Vos, Johannes G. [School of Chemical Sciences, Dublin City University (DCU), Glasnevin, Dublin 9 (Ireland); Dini, Danilo [Department of Chemistry, University of Rome “La Sapienza”, Piazzale Aldo Moro 5, 00185 Rome (Italy); Solar Energy Conversion Strategic Research Cluster, University College Dublin (UCD), Belfield, Dublin 4 (Ireland)

    2017-05-01

    Highlights: • NiO porous thin films were prepared via RDS technique. • NiO electrodes were characterized in a nitrile based electrochemical cell. • NiO electrodes were studied by means of XPS. • The XP spectra excluded the formation of phases other than NiO. • The presence of ClO{sub 4}{sup −} as charge balancing species was evidenced. - Abstract: Nanostructured nickel oxide (NiO) was deposited in the configuration of thin film (thickness, l = 2–6 μm) onto fluorine-doped tin oxide (FTO) substrates via plasma-assisted rapid discharge sintering (RDS). Electrochemical cycling of RDS NiO in 3-methoxy-propionitrile (3-MPN) revealed two characteristic peaks of NiO oxidation which were associated to the surface-confined redox processes Ni(II) → Ni(III) and Ni(III) → Ni(IV). Grazing angle X-ray photoelectron spectroscopy (XPS) was conducted ex-situ on NiO electrodes in both pristine and oxidized states. Oxidized NiO samples for XPS experiments were obtained in the potentiostatic mode through the polarization of NiO at its two characteristic potentials of oxidation. The XPS analysis allowed to ascertain the electronic structure of the nanoporous NiO framework, and verify the adsorption of perchlorate and chloride anions onto NiO surface due to the compensation of the charge stored in oxidized NiO. XPS also revealed that the spectrum within the region characteristic of Ni 2p ionization does not vary considerably with the state of charge of the nickel centres. This finding is in evident contrast to what has been observed for the same system when it undergoes electrochemical oxidation in aqueous electrolyte.

  5. Synthesis, photophysical, electrochemical and theoretical studies of the novel indolo[3,2-b]indole derivatives

    Science.gov (United States)

    Tian, Jinchang; Huang, Xin; Mao, Guijie; Xu, Feng; Chu, Wenyi; Sun, ZhiZhong

    2017-09-01

    A series of novel indolo[3,2-b]indole derivatives as blue-light-emitting materials were designed and synthesized by Pd (Ⅱ) catalyzed Suzuki coupling reaction in good yields. The thermal, photophysical, electrochemical properties of the derivatives were investigated and compared by introducing different terminal aromatic units into the target compounds. The results indicated that these new compounds exhibited high thermal stabilities, good solubility, stably blue fluorescent properties and good electronic transmission abilities. All the target compounds showed the potential to be used as blue fluorescent materials.

  6. Monitoring the electrochemical responses of neurotransmitters through localized surface plasmon resonance using nanohole array.

    Science.gov (United States)

    Li, Nantao; Lu, Yanli; Li, Shuang; Zhang, Qian; Wu, Jiajia; Jiang, Jing; Liu, Gang Logan; Liu, Qingjun

    2017-07-15

    In this study, a novel spectroelectrochemical method was proposed for neurotransmitters detection. The central sensing device was a hybrid structure of nanohole array and gold nanoparticles, which demonstrated good conductivity and high localized surface plasmon resonance (LSPR) sensitivity. By utilizing such specially-designed nanoplasmonic sensor as working electrode, both electrical and spectral responses on the surface of the sensor could be simultaneously detected during the electrochemical process. Cyclic voltammetry was implemented to activate the oxidation and recovery of dopamine and serotonin, while transmission spectrum measurement was carried out to synchronously record to LSPR responses of the nanoplasmonic sensor. Coupling with electrochemistry, LSPR results indicated good integrity and linearity, along with promising accuracy in qualitative and quantitative detection even for mixed solution and in brain tissue homogenates. Also, the detection results of other negatively-charged neurotransmitters like acetylcholine demonstrated the selectivity of our detection method for transmitters with positive charge. When compared with traditional electrochemical signals, LSPR signals provided better signal-to-noise ratio and lower detection limits, along with immunity against interference factors like ascorbic acid. Taking the advantages of such robustness, the coupled detection method was proved to be a promising platform for point-of-care testing for neurotransmitters. Copyright © 2016 Elsevier B.V. All rights reserved.

  7. Surface electrochemical control for the fine coal and pyrite separation. Technical progress report, October 1, 1989--December 31, 1989

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Wanxiong; Hu, Weibai; Wann, Jyi-Perng; Zhu, Ximeng; Wadsworth, M.E.; Bodily, D.M.

    1989-12-31

    Ongoing work includes the characterization of coal pyrites, the floatability evaluation of typical US coal samples, the flotation behavior of coal pyrites, the electrochemical measurement of the surface properties of coal pyrites, and the characterization of species produced at pyrite surfaces.

  8. Capacitance, charge dynamics, and electrolyte-surface interactions in functionalized carbide-derived carbon electrodes

    Directory of Open Access Journals (Sweden)

    Boris Dyatkin

    2015-12-01

    Full Text Available This study analyzed the dynamics of ionic liquid electrolyte inside of defunctionalized, hydrogenated, and aminated pores of carbide-derived carbon supercapacitor electrodes. The approach tailors surface functionalities and tunes nanoporous structures to decouple the influence of pore wall composition on capacitance, ionic resistance, and long-term cyclability. Quasi-elastic neutron scattering probes the self-diffusion properties and electrode-ion interactions of electrolyte molecules confined in functionalized pores. Room-temperature ionic liquid interactions in confined pores are strongest when the hydrogen-containing groups are present on the surface. This property translates into higher capacitance and greater ion transport through pores during electrochemical cycling. Unlike hydrogenated pores, aminated pores do not favorably interact with ionic liquid ions and, subsequently, are outperformed by defunctionalized surfaces.

  9. Electrochemical sensor for sensitive detection of paracetamol based on novel multi-walled carbon nanotubes-derived organic-inorganic material.

    Science.gov (United States)

    Hui, Junmin; Li, Wenjuan; Guo, Yanlei; Yang, Zhu; Wang, Yingxiong; Yu, Chao

    2014-03-01

    A new electrochemical sensor based on a novel organic-inorganic material (PNFCTs) was proposed for detection of paracetamol in this paper. First, PNFCTs were prepared with multi-walled carbon nanotubes (MWNTs) and a derivative of 3,4,9,10-perylenetetracarboxylic dianhydride (PTC-NH2) via cross-linking method. Then, PNFCTs were coated onto the surface of the glassy carbon electrode (GCE) to form porous organic conducting polymer films (PNFCTs/GCE), which could not only increase the loading of paracetamol efficiently but also provide an interface with exceptional electrical conductivity for paracetamol. Finally, gold nanoparticles (GNPs) were attached to the electrode surface through electrodepositing method, which obtained GNPs/PNFCTs/GCE electrode. The electrochemical behavior of paracetamol on GNPs/PNFCTs/GCE was explored by cyclic voltammetrys (CVs) and differential pulse voltammograms (DPVs). The results showed that the GNPs/PNFCTs/GCE exhibited excellent electrocatalytic activity to paracetamol, which should be attributed to remarkable properties of the new composite nanomaterials with porous nanostructure and exceptional electrical conductivity. The wide liner range and detection limit were 0.3-575 and 0.1 μM, respectively. Finally, it was successfully used to detect paracetamol in dilution human serum and commercial tablets. The sensor shows great promise for simple, sensitive, and selective detection paracetamol and provides a promising approach in paracetamol clinical research and overdose diagnostic applications.

  10. Ellipsometric and Electrochemical Characterization of Charge Transport in Electroactive Polymers and of the Surface Phase Produced by Electrochemical Activation of Glassy Carbon Electrodes

    Science.gov (United States)

    Kepley, Larry Joe

    1990-01-01

    In situ ellipsometry was used to study the electrodeposition of polymer films formed by oxidation of bipyrazine, polyvinylferrocene (PVF), and aniline; the deposition of a viologen-containing siloxane polymer (PQ^{2+/+}) formed by electroreduction of N,N^' -bis (-3-(trimethoxysilyl)propyl) -4,4^ '-bipyridinium dichloride (I) solutions and by spin-casting solutions of I; and the oxidation-dependent swelling of spin-cast films of two structurally similar, ferrocene-containing polyamides. Electrodeposited films displayed good optical characteristics (i.e., high reflectivity, uniform coverage, and homogeneity) for thicknesses up to 400 nm in some cases. Nonideal illipsometric behavior was observed when film morphology varied with film growth. The complex refractive index, film thickness, and the viologen and ferrocene concentrations in the films were measured as a function of oxidation state, both during depositions and after transferring coated-electrodes into blank electrolyte solutions. The voltammetry of the redox polymers was studied and charge-transport modeled by finite -difference simulations of charge diffusion and diffusion coupled to dimerization/monomerization reactions. Equations were derived for linear-sweep voltammetry of a reversible couple in equilibrium with its dimer in a thin-layer cell. Ellipsometric data during electrolysis of the redox films by potential sweeps and steps were compared to theoretical curves for diffusional transport to determine the mechanism of charge transport and to optically measure its rate. The influence of redox-induced thickness changes and solvent sorption on charge transport and voltammetric behavior is described. The electrochemical activation of glassy carbon electrodes for electrolysis of aromatic molecules, such as catechol and hydroquinone, was studied by combined ellipsometric and voltammetric measurements. Ellipsometry was used to detect the anodic growth of nearly transparent layer which activated the surface. X

  11. Surface-fluorinated proton-exchange membrane with high electrochemical durability for direct methanol fuel cells.

    Science.gov (United States)

    Lee, Chang Hyun; Lee, So Young; Lee, Young Moo; Lee, Sang Yun; Rhim, Ji Won; Lane, Ozma; McGrath, James E

    2009-05-01

    Random disulfonated poly(arylene ether sulfone)-silica nanocomposite (FSPAES-SiO2) membranes were physicochemically tuned via surface fluorination. Surface fluorination for 30 min converted about 20% of the C-H bonds on the membrane surface into C-F bonds showing hydrophobicity and electronegativity at the same time. The membranes with hydrophobic surface properties showed high dimensional stability and low methanol permeability when hydrated for direct methanol fuel cell applications. In particular, the surface enrichment of fluorine atoms led to anisotropic swelling behavior, associated with a stable electrode interface formation. Interestingly, in spite of the use of a random copolymer as a polymer matrix, the low surface free energy of the C-F bonds induced a well-defined continuous ionic channel structure, similar to those of multiblock copolymers. In addition to the morphological transition, fluorine atoms with high electron-withdrawing capability promoted the dissociation of sulfonic acid (-SO3H) groups. Consequently, FSPAES-SiO2 membranes exhibited improved proton conductivity. Thus, FSPAES-SiO2 membranes exhibited significantly improved single-cell performances (about 200%) at a constant voltage of 0.4 V in comparison with those of Nafion 117 and nonfluorinated membranes. Surprisingly, their good electrochemical performances were maintained with very low nonrecovery loss over the time period of 1400 h and interfacial resistances 380% times lower than those of conventional membrane-electrode assemblies comprising the control hydrocarbon membrane and a Nafion binder for the electrodes.

  12. An investigation of the electrochemical action of the epoxy zinc-rich coatings containing surface modified aluminum nanoparticle

    Science.gov (United States)

    Jalili, M.; Rostami, M.; Ramezanzadeh, B.

    2015-02-01

    Aluminum nanoparticle was modified with amino trimethylene phosphonic acid (ATMP). The surface characterization of the nanoparticles was done by X-ray photo electron spectroscopy (XPS), Fourier transform infrared spectroscopy (FTIR) and thermal gravimetric analysis. The influence of the replacement of 2 wt% of zinc dust in the standard zinc-rich epoxy coating by nanoparticles on the electrochemical action of the coating was studied by electrochemical impedance spectroscopy (EIS) and salt spray tests. The morphology and phase composition of the zinc rich paints were evaluated by X-ray diffraction (XRD) and filed-emission scanning electron microscopy (FE-SEM). Results showed that the ATMP molecules successfully adsorbed on the surface of Al nanoparticles. Results obtained from salt spray and electrochemical measurements revealed that the addition of surface modified nanoparticles to the zinc rich coating enhanced its galvanic action and corrosion protection properties.

  13. Advanced Electrochemical Machining (ECM) for tungsten surface micro-structuring in blanket applications

    Energy Technology Data Exchange (ETDEWEB)

    Holstein, Nils, E-mail: nils.holstein@kit.edu [Karlsruhe Institute of Technology, Hermann-von-Helmholtz-Platz 1, D-76344 Eggenstein-Leopoldshafen, Baden-Württemberg (Germany); Krauss, Wolfgang; Konys, Jürgen [Karlsruhe Institute of Technology, Hermann-von-Helmholtz-Platz 1, D-76344 Eggenstein-Leopoldshafen, Baden-Württemberg (Germany); Heuer, Simon; Weber, Thomas [Research Center Jülich, Institute of Energy- and Climate Research – Plasma Physics (IEK-4), D-52425 Jülich (Germany)

    2016-11-01

    Highlights: • Electrochemical Machining is an appropriate tool for tungsten shaping. • Progress in shaping achieved by combination of ECM with advanced micro-lithography. • Application in First Wall for connection of plasma facing material to breeder blanket. • Successful development of adhesion promotors by ECM for plasma spraying interlayers. • Microstructure electrochemical manufacturing of tungsten in sizes of 100 μm achieved. - Abstract: Plasma facing components for fusion applications must have to exhibit long-term stability under extreme physical conditions, and therefore any material imperfections caused by mechanical and/or thermal stresses in the shaping processes cannot be tolerated due to a high risk of possible technical failures under fusion conditions. To avoid such defects, the method of Electrochemical Machining (ECM) enables a complete defect-free processing of removal of tungsten material during the desired shaping, also for high penetration depths. Furthermore, supported by lithographic mask pretreatment, three-dimensional distinct geometric structures can be positive-imaged via the directional galvanic dissolution applying M-ECM process into the tungsten bulk material. New required applications for tungsten components, e.g. as adhesion promotors in W-surfaces to enable sure grip and bonding of thick plasma-spraying layers for blanket components, will define the way of further miniaturization of well-established millimeter dimensioned M-ECM shaping processes to dimensions of 100 μm and furthermore down to 50 μm. Besides current M-ECM limits the article describes inevitable needs of further developments for mask resists, mask materials and the resulting ECM parameters, to reach the needed accuracy in tungsten microstructure. The achieved progress and observed correlations of processing parameters will be manifested by produced demonstrators made by the new “μM”-ECM process.

  14. Interaction of Two Water Soluble Heterocyclic Hydrazones on Copper in Nitric Acid: Electrochemical, Surface Morphological, and Quantum Chemical Investigations

    Directory of Open Access Journals (Sweden)

    Vinod P. Raphael

    2016-01-01

    Full Text Available Two novel heterocyclic compounds (E-2-(1-(pyridin-3-ylethylidenehydrazinecarbothioamide (3APTSC and (E-3-(1-(2-phenylhydrazonoethylpyridine (3APPH derived from 1-(pyridin-3-ylethanone were synthesized and characterized by various spectroscopic techniques. The corrosion inhibition efficacies of these compounds on copper in 0.1 M HNO3 were screened by electrochemical corrosion monitoring techniques such as potentiodynamic polarization studies and impedance spectroscopy. Investigations clearly established that 3APPH displayed higher corrosion inhibition efficiency on Cu than 3APTSC at all concentrations. The mechanism of inhibition was verified with the help of adsorption isotherms. 3APTSC and 3APPH obeyed Langmuir adsorption isotherm on Cu surface. Thermodynamic parameters such as adsorption equilibrium constant (Kads and free energy of adsorption (ΔGads were also evaluated. Potentiodynamic polarization investigations confirmed that the 3APTSC and 3APPH act as mixed type inhibitors. Surface analysis of the metal specimens was performed by scanning electron microscopy. Energy of HOMO and LUMO, their difference, number of electrons transferred, electronegativity, chemical hardness, and so forth were evaluated by quantum chemical studies. Agreeable correlation was observed between the results of quantum chemical calculations and other corrosion monitoring techniques.

  15. Surface-reconstructed Cu Electrode via a Facile Electrochemical Anodization-Reduction Process for Low Overpotential CO 2 reduction

    KAUST Repository

    Min, Shixiong

    2017-03-21

    A high-surface-area Cu electrode, fabricated by a simple electrochemical anodization-reduction method, exhibits high activity and selectivity for CO2 reduction at low overpotential in 0.1 M KHCO3 solution. A faradaic efficiency of 37% for HCOOH and 27% for CO production was achieved with the current density of 1.5 mA cm-2 at −0.64 V vs. RHE, much higher than that of polycrystalline Cu. The enhanced catalytic performance is a result of the formation of the high electrochemical active surface area and high density of preferred low-index facets.

  16. Preparation and characteristics of the sulfonated chitosan derivatives electrodeposited onto 316l stainless steel surface.

    Science.gov (United States)

    Huang, Ye; Peng, Guangjia; Chen, Bin; Yong, Ping; Yao, Nan; Yang, Liming; Pirraco, Rogério P; Reis, Rui L; Chen, Jie

    2018-02-01

    In order to ameliorate the properties of corrosion resistance and achieve applications in anti-biofouling of 316L stainless steel (SS), a sulfated derivative of chitosan was deposited onto stainless steel surface by an electrochemical method. In detail, chitosan-catechol (CS-CT) was synthesised in the hydrochloric acid solution by the Mannich reaction and then electrodeposited on the surface of the polished 316L stainless steel. The chitosan-catechol deposited SS sample was further modified with maleic anhydride and sulfite. The grafting progress was monitored by FTIR, UV spectrophotometer and X-ray photoelectron spectroscopy. Hydrophilicity and corrosion resistance of modified SS were characterized by water contact angle measurements, Tafel curves and electrochemical impedance spectroscopy. The morphology of the SS surface before and after the modification was investigated by atomic force microscopy and scanning electron microscope. Further, the anti-biofouling performance in terms of the anti-adsorption protein and anti-bacteria effects of all modified SS samples were estimated, and the modified 316L exhibits the capability of lower protein adsorption and improved antibacterial effect.

  17. Electrochemically assisted deposition of strontium modified magnesium phosphate on titanium surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Meininger, M. [Department for Functional Materials in Medicine and Dentistry, University of Würzburg, Pleicherwall 2, D-97070 Würzburg (Germany); Wolf-Brandstetter, C. [Max Bergmann Center for Biomaterials, Technical University of Dresden, Budapester Straße 27, D-01069 Dresden (Germany); Zerweck, J.; Wenninger, F.; Gbureck, U.; Groll, J. [Department for Functional Materials in Medicine and Dentistry, University of Würzburg, Pleicherwall 2, D-97070 Würzburg (Germany); Moseke, C., E-mail: claus.moseke@fmz.uni-wuerzburg.de [Department for Functional Materials in Medicine and Dentistry, University of Würzburg, Pleicherwall 2, D-97070 Würzburg (Germany)

    2016-10-01

    Electrochemically assisted deposition was utilized to produce ceramic coatings on the basis of magnesium ammonium phosphate (struvite) on corundum-blasted titanium surfaces. By the addition of defined concentrations of strontium nitrate to the coating electrolyte Sr{sup 2+} ions were successfully incorporated into the struvite matrix. By variation of deposition parameters it was possible to fabricate coatings with different kinetics of Sr{sup 2+} into physiological media, whereas the release of therapeutically relevant strontium doses could be sustained over several weeks. Morphological and crystallographic examinations of the immersed coatings revealed that the degradation of struvite and the release of Sr{sup 2+} ions were accompanied by a transformation of the coating to a calcium phosphate based phase similar to low-crystalline hydroxyapatite. These findings showed that strontium doped struvite coatings may provide a promising degradable coating system for the local application of strontium or other biologically active metal ions in the implant–bone interface. - Highlights: • Sr-doped struvite coatings have been deposited on titanium by electrochemically assisted deposition. • Sr content can be adjusted by means of process time, current density and pulse mode. • Sr-doped coatings release therapeutically relevant Sr doses in physiological media for several weeks. • During immersion in physiological media Sr-doped struvite coatings transform into a low crystalline calcium phosphate phase.

  18. Surface electrochemical control for fine coal and pyrite separation. Final report

    Energy Technology Data Exchange (ETDEWEB)

    Wadsworth, M.E.; Bodily, D.M.; Hu, Weibai; Chen, Wanxiong; Huang, Qinping; Liang, Jun; Riley, A.M.; Li, Jun; Wann, Jyi-Perng; Zhong, Tingke; Zhu, Ximeng

    1993-01-20

    Laboratory flotation tests were carried out on three coals and on coal pyrite. Floatability measurements included natural floatability, flotation with a xanthate collector and salt flotation. The ranking of the floatability of the three coals were: Upper Freeport > Pittsburgh > Illinois. The floatability of mineral pyrite and coal pyrite increased markedly with xanthate concentration, but decreased with increased pH. In general, coal pyrite was more difficult to float than mineral pyrite. This was attributed to the presence of surface carbonaceous and mineral matter, since floatability of coal pyrite improved by acid pretreatment. Flotation tests demonstrated that the floatability of coal and mineral pyrite was greatly enhanced by the presence of an electrolyte. Flotation was also enhanced by the addition of modifiers such as CuSO{sub 4}, Na{sub 2}S, CO{sub 2} and EDTA. Lime additions markedly reduced the floatability of coal pyrite. Enhanced floatability of coal pyrite resulted when the pyrite was anodically oxidized in a specially constructed electrochemical flotation cell Pretreatment in potential ranges previously observed for polysulfide and sulfur film formation resulted in the enhanced floatability. While interesting trends and influences, both chemical and electrochemical, markedly improved the floatability of coal, there is little hope for reverse flotation as an effective technology for coal/coal-pyrite separations. The effects of poor liberation and entrainment appear overriding.

  19. Electrochemical analysis of the UV treated bactericidal Ti6Al4V surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Pacha-Olivenza, Miguel A. [Networking Research Center on Bioengineering, Biomaterials and Nanomedicine (CIBER-BBN) (Spain); Department of Applied Physics, Faculty of Science, University of Extremadura, Av. Elvas s/n, 06071 Badajoz (Spain); Gallardo-Moreno, Amparo M., E-mail: amparogm@unex.es [Department of Applied Physics, Faculty of Science, University of Extremadura, Av. Elvas s/n, 06071 Badajoz (Spain); Networking Research Center on Bioengineering, Biomaterials and Nanomedicine (CIBER-BBN) (Spain); Vadillo-Rodríguez, Virginia; González-Martín, M. Luisa [Department of Applied Physics, Faculty of Science, University of Extremadura, Av. Elvas s/n, 06071 Badajoz (Spain); Networking Research Center on Bioengineering, Biomaterials and Nanomedicine (CIBER-BBN) (Spain); Pérez-Giraldo, Ciro [Department of Microbiology, Faculty of Medicine, University of Extremadura, Av. Elvas s/n, 06071 Badajoz (Spain); Networking Research Center on Bioengineering, Biomaterials and Nanomedicine (CIBER-BBN) (Spain); Galván, Juan C. [National Centre for Metallurgical Research (CENIM-CSIC), Av. Gregorio del Amo 8, 28040-Madrid (Spain)

    2013-04-01

    This research investigates in detail the bactericidal effect exhibited by the surface of the biomaterial Ti6Al4V after being subjected to UV-C light. It has been recently hypothesized that small surface currents, occurring as a consequence of the electron–hole pair recombination taking place after the excitation process, are behind the bactericidal properties displayed by this UV-treated material. To corroborate this hypothesis we have used different electrochemical techniques, such as electrochemical impedance spectroscopy (EIS), potentiodynamic polarization plots and Mott–Schottky plots. EIS and Mott–Schottky plots have shown that UV-C treatment causes an initial increase on the surface electrical conduction of this material. In addition, EIS and polarization plots demonstrated that higher corrosion currents occur at the UV treated than at the non-irradiated samples. Despite this increase in the corrosion currents, EIS has also shown that such currents are not likely to affect the good stability of this material oxide film since the irradiated samples completely recovered the control values after being stored in dark conditions for a period not longer than 24 h. These results agree with the already-published in vitro transitory behavior of the bactericidal effect, which was shown to be present at initial times after the biomaterial implantation, a crucial moment to avoid a large number of biomaterial associated infections. Highlights: ► Bactericidal response of UV-treated Ti6Al4V is explained through electrochemistry. ► There is an increase in the superficial electrical conduction after UV-treatment. ► Higher corrosion currents for UV-treated against non-UV-treated samples are shown. ► EIS shows the recuperation on irradiated samples in agreement with microbial tests.

  20. Effect of passive film on electrochemical surface treatment for indium tin oxide

    Energy Technology Data Exchange (ETDEWEB)

    Wu, Yung-Fu, E-mail: gausswu@mail.mcut.edu.tw [Department of Chemical Engineering, MingChi University of Technology, 84 Gungjuan Rd., Taishan, Taipei 24301, Taiwan (China); Chen, Chi-Hao [Department of Chemical Engineering, MingChi University of Technology, 84 Gungjuan Rd., Taishan, Taipei 24301, Taiwan (China)

    2013-02-15

    Highlights: Black-Right-Pointing-Pointer Oxalic, tartaric, and citric acid baths accompanying with applied voltages were used to treat the ITO surface. Black-Right-Pointing-Pointer We investigated the changes in ITO surfaces by examining the potentiodynamic behavior of ITO films. Black-Right-Pointing-Pointer AFM analysis showed the formation of a passive layer could assist to planarize surface. Black-Right-Pointing-Pointer XPS analysis indicated this passive layer was mainly composed of SnO{sub 2.} Black-Right-Pointing-Pointer A better planarization was obtained by treating in 3.0 wt.% tartaric acid at 0.5 V due to weak complexation strength. - Abstract: Changes in indium tin oxide (ITO) film surface during electrochemical treatment in oxalic acid, tartaric acid, and citric acid were investigated. Controlling the voltage applied on ITO film allows the formation of a passive layer, effectively protecting the film surface. X-ray photoelectron spectrometry showed that the passive layer composition was predominantly SnO{sub 2} in tartaric acid, while a composite of tin oxide and tin carboxylate in citric or oxalic acid. Even though the passive films on ITO surface generated in these organic acids, the indium or tin could complex with the organic acid anions, enhancing the dissolution of ITO films. The experimental results show that the interaction between the dissolution and passivation could assist to planarize the ITO surface. We found that the optimal treatment at 0.5 V in 3 wt.% tartaric acid could provide the ITO surface with root-mean-squared roughness less than 1.0 nm, due to the weak complexing characteristics of tartaric acid.

  1. Electrochemical behavior of a nitrobenzenesulfonyl derivative of aniline in aqueous solution

    OpenAIRE

    Boldrin Zanoni, M. V. [UNESP; Rosa, I.L.V.; Pesquero, C. R.; Stradiotto, Nelson Ramos [UNESP

    1997-01-01

    The electrochemical behavior of aniline protected by a nitrobenzene sulphonyl group in aqueous solution at a mercury electrode is reported. At pH 11). Controlled potential electrolysis confirms that the reduction of the nitro group in a four-electron step to N-phenyl-4-hydroxylamine sulphonamide is a...

  2. Effects of shot peening stand-off distance on electrochemical properties for surface modification of ALBC3 alloy

    Energy Technology Data Exchange (ETDEWEB)

    Han, Minsu; Kim, Seongjong [Mokpo Maritime Univ., Mokpo (Korea, Republic of); Hyun, Koangyong [Nagoya Univ., Nagoya (Japan)

    2013-05-15

    In the case of casting materials or ductile materials for marine equipment, it is common to employ a surface modification for achieving cost reduction and improvement in strength. In particular, aluminium bronze ALBC3 exhibits excellent corrosion resistance, and thus widely used for marine application. However, application of the material under high-velocity seawater flow may induce electrochemical corrosion damage and physical damage such as cavitation erosion, leading to shorter service life of equipment. In this study, surface modification was carried out on ALBC3 alloy for different shot peening stand-off distances, and the physical hardness and electrochemical characteristics before and after modification were investigated. The results in each case showed the hardness increase in comparison with non-peened specimen, and the maximum hardness improvement(50 %) was found in 10 cm of shot-peening stand-off distance. It is observed that the electrochemical characteristics were irrelevant to application of shot peening.

  3. Influence of the surface finishing on electrochemical corrosion characteristics of AISI 316L stainless steel

    Directory of Open Access Journals (Sweden)

    Sylvia Dundeková

    2015-05-01

    Full Text Available Stainless steels from 316 group are very often and successfully uses for medical applications where the good mechanical and chemical properties in combination with non-toxicity of the material assure its safe and long term usage. Corrosion properties of AISI 361L stainless steel are strongly influenced by surface roughness and treatment of the engineering parts (specimens and testing temperature. Electrochemical characteristics of ground, mechanically polished and passivated AISI 316L stainless steel specimens were examined with the aim to identify the polarization resistance evolution due to the surface roughness decrease. Results obtained on mechanically prepared specimens where only natural oxide layer created due to the exposure of the material to the corrosion environment was protecting the materials were compared to the passivated specimens with artificial oxide layer. Also the influence of temperature and stabilization time before measurement were taken into account when discussing the obtained results. Positive influence of decreasing surface roughness was obtained as well as increase of polarization resistance due to the chemical passivation of the surface. Increase of the testing temperature and short stabilization time of the specimen in the corrosion environment were observed negatively influencing corrosion resistance of AISI 316L stainless steel.

  4. Electrochemical measurements for the corrosion inhibition of mild steel in 1 M hydrochloric acid by using an aromatic hydrazide derivative

    Directory of Open Access Journals (Sweden)

    P. Preethi Kumari

    2017-07-01

    Full Text Available The influence of an aromatic hydrazide derivative, 2-(3,4,5-trimethoxybenzylidene hydrazinecarbothioamide (TMBHC as corrosion inhibitor on mild steel in 1 M hydrochloric acid was studied by Tafel polarization and electrochemical impedance spectroscopy (EIS technique. The results showed that the inhibition efficiency (% IE of TMBHC increased with increasing inhibitor concentrations and also with increase in temperatures. TMBHC acted as a mixed type of inhibitor and its adsorption on mild steel surface was found to follow Langmuir’s adsorption isotherm. The evaluation of thermodynamic and activation parameters indicated that the adsorption of TMBHC takes place through chemisorption. The formation of protective film was further confirmed by scanning electron microscopy (SEM.

  5. Polystyrene sphere monolayer assisted electrochemical deposition of ZnO nanorods with controlable surface density

    Energy Technology Data Exchange (ETDEWEB)

    Ramirez, D., E-mail: daniel.ramirez@ucv.c [Laboratorio de Electroquimica, Pontificia Universidad Catolica de Valparaiso, Valparaiso (Chile); Gomez, H. [Laboratorio de Electroquimica, Pontificia Universidad Catolica de Valparaiso, Valparaiso (Chile); Lincot, D. [Institute de Recherche et Developpement sur l' Energie Photovoltaique-IRDEP, 6 Quai Watier 78401, Chatou Cedex (France)

    2010-02-15

    In this paper we report the zinc oxide nanorods (ZnO NRs) growth by electrochemical deposition onto polycrystalline gold electrodes modified with assemblies of polystyrene sphere monolayers (PSSMs). Growth occurs through the interstitial spaces between the hexagonally close packed spheres. ZnO NRs nucleate in the region where three adjacent spheres leave a space, being able to grow and projected over the PSSMs. The nanorod surface density (N{sub NR}) shows a linear dependence with respect to a PS sphere diameter selected. XRD analysis shows these ZnO NRs are highly oriented along the (0 0 2) plane (c-axis). This open the possibility to have electronic devices with mechanically supported nanometric materials.

  6. Synthesis and electrochemical property of Bi2Se3 nanotubes with laminar surface.

    Science.gov (United States)

    Mao, Shuling; Zhang, Shengyi; Niu, Helin; Song, Jiming; Jin, Baokang; Wu, Jieying; Tian, Yupeng

    2011-03-01

    A novel hydrothermal method has been developed for the preparation of Bi2Se3 nanotubes with the laminar surface. The method is based on the template-engaged synthesis in which the as-prepared Se nanotubes were used as template reagent. The morphology, constitution and crystalline phase of the products as-obtained were characterized by SEM, XRD and XPS. On the basis of a series of experiments and characterizations, the effect factors (such as the reaction temperature and the atom ratio of Bi and Se in the precursors) and the formation mechanism of the Bi2Se3 nanotubes were discussed. Furthermore, the electrochemical property of the Bi2Se3 nanotubes was determined by the voltammetric technique, and the significant results were obtained.

  7. Development of scanning electrochemical microscopy for the investigation of photocatalysis at semiconductor surfaces

    CERN Document Server

    Fonseca, S M M C D

    2002-01-01

    This thesis is concerned with the development and application of scanning electrochemical microscopy (SECM) to investigate interfacial photoelectrochemical processes occurring at supported TiO sub 2 surfaces. The new SECM approach, involving both amperometric and potentiometric electrodes, was used to monitor interfacial photoprocesses with high spatial resolution. A new in situ photoelectrochemical approach to chemical actinometry has been developed and used to determine the light flux through a quartz fibre employed in the SECM system. In this system an ultramicroelectrode (UME) probe is positioned with high precision at a known distance close to a TiO sub 2 -coated fibre and used to detect reactants or products of the ongoing photodegradation process. The microelectrochemical actinometry approach was developed using the well-known liquid phase potassium ferrioxalate actinometer. The approach involved recording the steady-state current for Fe(lll) reduction at an SECM tip positioned close to the fibre. A st...

  8. [The effect of epigallocatechin gallate (EGCG) on the surface properties of nickel-chromium dental casting alloys after electrochemical corrosion].

    Science.gov (United States)

    Qiao, Guang-yan; Zhang, Li-xia; Wang, Jue; Shen, Qing-ping; Su, Jian-sheng

    2014-08-01

    To investigate the effect of epigallocatechin gallate (EGCG) on the surface properties of nickel-chromium dental alloys after electrochemical corrosion. The surface morphology and surface structure of nickel-chromium dental alloys were examined by stereomicroscope and scanning electron microscopy before and after electrochemical tests in 0 g/L and 1.0 g/L EGCG artificial saliva. The surface element component and chemical states of nickel-chromium dental alloys were analyzed by X-ray photoelectron spectrograph after electrochemical tests in 0 g/L and 1.0 g/L EGCG artificial saliva. More serious corrosion happened on the surface of nickel-chromium alloy in 1.0 g/L EGCG artificial saliva than in 0 g/L EGCG. The diameters of corrosion pits were smaller, and the dendrite structure of the alloy surface was not affected in 0 g/L EGCG. While the diameters of corrosion pits were larger, the dendritic interval of the alloy surface began to merge, and the dendrite structure was fuzzy in 1.0 g/L EGCG. In addition, the O, Ni, Cr, Be, C and Mo elements were detected on the surface of nickel-chromium alloys after sputtered for 120 s in 0 g/L EGCG and 1.0 g/L EGCG artificial saliva after electrochemical corrosion, and the surface oxides were mainly NiO and Cr(2)O(3). Compared with 0 g/L EGCG artificial saliva, the content of O, NiO and Cr(2)O(3) were lower in 1.0 g/L EGCG. The results of surface morphology and the corrosion products both show that the corrosion resistance of nickel-chromium alloys become worse and the oxide content of corrosion products on the surface reduce in 1.0 g/L EGCG artificial saliva.

  9. Synthesis, structural study and electrochemical properties of copper(II complexes derived from benzene- and p-toluenesulphonylhydrazones

    Directory of Open Access Journals (Sweden)

    A. REGUIG

    2003-02-01

    Full Text Available The synthesis and characterization of benzene- and p-toluenesulphonylhydrazones derived from salicylaldehyde and 2-hydroxy-1-naphthaldehyde and their Cu(II complexes are reported. The compounds were characterized on the basis of elemental analyses, electronic and IR spectra, magnetic moments, and conductance measurements. The electrochemical behavior of the Cu(II complexes was investigated in DMSO by cyclic voltammetry (CV, rotating disc electrode (RDE and coulometry. The oxidative polymerization of the copper complexes on a glassy carbon electrode was carried out in DMSO.

  10. Kinetic study of electrochemically induced michael reactions of o-quinones with Meldrum's acid derivatives. Synthesis of highly oxygenated catechols.

    Science.gov (United States)

    Nematollahi, D; Shayani-jam, H

    2008-05-02

    Electrochemical oxidation of catechols has been studied in the presence of Meldrum's acid derivatives as nucleophiles in aqueous solution, by means of cyclic voltammetry and controlled-potential coulometry. Catechols in the Michael addition reaction react with Meldrum's acids to form adducts that can undergo electrooxidation. Such products were obtained in good yields as confirmed by controlled potential electrosynthesis. Such products can be generated in aqueous solutions by means of electrosynthesis, using a carbon electrode in an undivided cell. Furthermore, the homogeneous rate constants of the chemical reaction interposed between electron transfers were estimated by comparing the experimental cyclic voltammetric curves with the digitally simulated ones.

  11. Novel electrochemical redox-active species: one-step synthesis of polyaniline derivative-Au/Pd and its application for multiplexed immunoassay.

    Science.gov (United States)

    Wang, Liyuan; Feng, Feng; Ma, Zhanfang

    2015-11-18

    Electrochemical redox-active species play crucial role in electrochemically multiplexed immunoassays. A one-pot method for synthesizing four kinds of new electrochemical redox-active species was reported using HAuCl4 and Na2PdCl4 as dual oxidating agents and aniline derivatives as monomers. The synthesized polyaniline derivative-Au/Pd composites, namely poly(N-methyl-o-benzenediamine)-Au/Pd, poly(N-phenyl-o-phenylenediamine)-Au/Pd, poly(N-phenyl-p-phenylenediamine)-Au/Pd and poly(3,3',5,5'-tetramethylbenzidine)-Au/Pd, exhibited electrochemical redox activity at -0.65 V, -0.3 V, 0.12 V, and 0.5 V, respectively. Meanwhile, these composites showed high H2O2 electrocatalytic activity because of the presence of Au/Pd. The as-prepared composites were used as electrochemical immunoprobes in simultaneous detection of four tumor biomarkers (carcinoembryonic antigen (CEA), carbohydrate antigen 19-9 (CA199), carbohydrate antigen 72-4 (CA724), and alpha fetoprotein (AFP)). This immunoassay shed light on potential applications in simultaneous gastric cancer (related biomarkers: CEA, CA199, CA724) and liver cancer diagnosis (related biomarkers: CEA, CA199, AFP). The present strategy to the synthesize redox species could be easily extended to other polymers such as polypyrrole derivatives and polythiophene derivatives. This would be of great significance in the electrochemical detection of more analytes.

  12. Novel electrochemical redox-active species: one-step synthesis of polyaniline derivative-Au/Pd and its application for multiplexed immunoassay

    Science.gov (United States)

    Wang, Liyuan; Feng, Feng; Ma, Zhanfang

    2015-11-01

    Electrochemical redox-active species play crucial role in electrochemically multiplexed immunoassays. A one-pot method for synthesizing four kinds of new electrochemical redox-active species was reported using HAuCl4 and Na2PdCl4 as dual oxidating agents and aniline derivatives as monomers. The synthesized polyaniline derivative-Au/Pd composites, namely poly(N-methyl-o-benzenediamine)-Au/Pd, poly(N-phenyl-o-phenylenediamine)-Au/Pd, poly(N-phenyl-p-phenylenediamine)-Au/Pd and poly(3,3’,5,5’-tetramethylbenzidine)-Au/Pd, exhibited electrochemical redox activity at -0.65 V, -0.3 V, 0.12 V, and 0.5 V, respectively. Meanwhile, these composites showed high H2O2 electrocatalytic activity because of the presence of Au/Pd. The as-prepared composites were used as electrochemical immunoprobes in simultaneous detection of four tumor biomarkers (carcinoembryonic antigen (CEA), carbohydrate antigen 19-9 (CA199), carbohydrate antigen 72-4 (CA724), and alpha fetoprotein (AFP)). This immunoassay shed light on potential applications in simultaneous gastric cancer (related biomarkers: CEA, CA199, CA724) and liver cancer diagnosis (related biomarkers: CEA, CA199, AFP). The present strategy to the synthesize redox species could be easily extended to other polymers such as polypyrrole derivatives and polythiophene derivatives. This would be of great significance in the electrochemical detection of more analytes.

  13. Anisotropic surface hole-transport property of triphenylamine-derivative single crystal prepared by solution method

    Energy Technology Data Exchange (ETDEWEB)

    Umeda, Minoru, E-mail: mumeda@vos.nagaokaut.ac.jp [Nagaoka University of Technology, Kamitomioka, Nagaoka, Niigata 940-2188 (Japan); Katagiri, Mitsuhiko; Shironita, Sayoko [Nagaoka University of Technology, Kamitomioka, Nagaoka, Niigata 940-2188 (Japan); Nagayama, Norio [Nagaoka University of Technology, Kamitomioka, Nagaoka, Niigata 940-2188 (Japan); Ricoh Company, Ltd., Nishisawada, Numazu, Shizuoka 410-0007 (Japan)

    2016-12-01

    Highlights: • A hole transport molecule was investigated based on its electrochemical redox characteristics. • The solubility and supersolubility curves of the molecule were measured in order to prepare a large crystal. • The polarization micrograph and XRD results revealed that a single crystal was obtained. • An anisotropic surface conduction, in which the long-axis direction exceeds that of the amorphous layer, was observed. • The anisotropic surface conduction was well explained by the molecular stacked structure. - Abstract: This paper reports the anisotropic hole transport at the triphenylamine-derivative single crystal surface prepared by a solution method. Triphenylamine derivatives are commonly used in a hole-transport material for organic photoconductors of laser-beam printers, in which the materials are used as an amorphous form. For developing organic photovoltaics using the photoconductor’s technology, preparation of a single crystal seems to be a specific way by realizing the high mobility of an organic semiconductor. In this study, a single crystal of 4-(2,2-diphenylethenyl)-N,N-bis(4-methylphenyl)-benzenamine (TPA) was prepared and its anisotropic hole-transport property measured. First, the hole-transport property of the TPA was investigated based on its chemical structure and electrochemical redox characteristics. Next, a large-scale single crystal formation at a high rate was developed by employing a solution method based on its solubility and supersolubility curves. The grown TPA was found to be a single crystal based on the polarization micrograph observation and crystallographic analysis. For the TPA single crystal, an anisotropic surface conduction was found, which was well explained by its molecular stack structure. The measured current in the long-axis direction is one order of magnitude greater than that of amorphous TPA.

  14. Investigation on Electrochemical Properties of Polythiophene Nanocomposite with Graphite Derivatives as Supercapacitor Material on Breath Figure-Decorated PMMA Electrode

    Science.gov (United States)

    Azimi, Mona; Abbaspour, Mohsen; Fazli, Ali; Setoodeh, Hamideh; Pourabbas, Behzad

    2018-03-01

    Breath figures have been formed by the direct breath figure method on polymethyl methacrylate electrode sand hexagonal oriented holes with 0.5- to 10- μm2 surface area have been created. Deposition of materials on the electrodes has been performed by the spray-coating method. polythiophene (PTh) nanoparticles, polythiophene-graphene oxide (PTh-GO) and polythiophene-reduced graphene oxide (PTh-G) nanocomposites were synthesized by emulsion polymerization, while characterization of synthetic materials have been carried out by Fourier transform infrared, Χ-ray diffraction, transmission electron microscopy, UV-Vis spectroscopy and field emission scanning electron microscopy techniques. Also, the electrochemical properties of the designed electrodes were investigated by cyclic voltammetry, galvanostatic charge-discharge and electrochemical impedance spectroscopy techniques. Specific capacitance of porous electrodes coated by PTh nanoparticles, PTh-GO and PTh-G nanocomposites were calculated from cyclic voltammetry curves at 5 mV/s scan rate, andthe values are 3.5 F/g, 16.39 F/g, and 28.68 F/g, respectively. Also, the energy density of each electrode at 5 mV/s scan rate has been calculated and the results show that incorporation of GO and G nanolayers with PTh nanoparticles enhances the electrochemical properties of electrodes.

  15. Controlled amino-functionalization by electrochemical reduction of bromo and nitro azobenzene layers bound to Si(111) surfaces

    NARCIS (Netherlands)

    Ullien, D.; Thüne, P.C.; Jager, W.F.; Sudhölter, E.J.R.; De Smet, L.C.P.M.

    2014-01-01

    4-Nitrobenzenediazonium (4-NBD) and 4-bromobenzenediazonium (4-BBD) salts were grafted electrochemically onto H-terminated, p-doped silicon (Si) surfaces. Atomic force microscopy (AFM) and ellipsometry experiments clearly showed layer thicknesses of 2–7 nm, which indicate multilayer formation.

  16. Constructing Functional Ionic Membrane Surface by Electrochemically Mediated Atom Transfer Radical Polymerization

    Directory of Open Access Journals (Sweden)

    Fen Ran

    2016-01-01

    Full Text Available The sodium polyacrylate (PAANa contained polyethersulfone membrane that was fabricated by preparation of PES-NH2 via nonsolvent phase separation method, the introduction of bromine groups as active sites by grafting α-Bromoisobutyryl bromide, and surface-initiated electrochemically atom transfer radical polymerization (SI-eATRP of sodium acrylate (AANa on the surface of PES membrane. The polymerization could be controlled by reaction condition, such as monomer concentration, electric potential, polymerization time, and modifier concentration. The membrane surface was uniform when the monomer concentration was 0.9 mol/L, the electric potential was −0.12 V, the polymerization time was 8 h, and the modifier concentration was 2 wt.%. The membrane showed excellent hydrophilicity and blood compatibility. The water contact angle decreased from 84° to 68° and activated partial thromboplastin increased from 51 s to 84 s after modification of the membranes.

  17. Electrochemical structuring of mechanically activated n-InP(100) surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Hueppe, M.; Schlierf, U.; Schmuki, P. [Department of Materials Science, LKO, University of Erlangen-Nuernberg, Martensstrasse 7, 91058 Erlangen (Germany); Gassiloud, R. [Department of Materials Science, LKO, University of Erlangen-Nuernberg, Martensstrasse 7, 91058 Erlangen (Germany); Materials Measurement Research Group, Swiss Federal Laboratory for Materials Testing and Research (EMPA), Feuerwerkstrasse 39, 3602 Thun (Switzerland); Michler, J. [Materials Measurement Research Group, Swiss Federal Laboratory for Materials Testing and Research (EMPA), Feuerwerkstrasse 39, 3602 Thun (Switzerland)

    2005-06-01

    Localized pore formation on n-InP(100) surfaces under anodic polarization in 1M HCl were created and controlled by a two steps approach. First, scratches in the nanometer scale have been applied mechanically, using a Nano-Indenter. These scratches represent activated sites for pore growth due to their lowered electrochemical pore formation potential (U{sub bd,activated}), which is significantly cathodic to the formation potential on intact surfaces U{sub bd} (U{sub bd,intact}). Thus, a potential window can be defined between U{sub bd,activated} and U{sub bd,intact}, where anodic polarization in 1M HCl leads to selective pore formation follows, at a potential that is inside those window. Characterization by scanning electron microscopy shows that pore formation occurs only at the activated sites. Furthermore, both broadening and morphology of the pores depend strongly on the force load during the scratching process. Analysis of the scratched surface has been carried out before and after etching, using atomic force microscopy (AFM). The results clearly show that the porous region is significantly wider than the originally scratched region - this can be ascribed to dislocation formation in the vicinity of the scratch. (copyright 2005 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  18. Pitting inhibition of stainless steel by surfactants: an electrochemical and surface chemical approach.

    Science.gov (United States)

    Wei, Zhenqiang; Duby, Paul; Somasundaran, P

    2003-03-01

    Pitting corrosion of stainless steels causes tremendous damage in terms of material loss and resulting accidents. Organic surfactants have been tried as pitting inhibitors but the understanding of the inhibition mechanisms is mainly speculative. In the present study the inhibition of the pitting corrosion of 304 stainless steel by N-lauroylsarcosine sodium salt (NLS) in 0.1 M NaCl solutions at neutral pH was studied using an approach that combines surface chemical techniques with electrochemical ones. It was found that NLS increases the pitting resistance of 304 stainless steel, with possible complete inhibition at high NLS concentration (30 mM). Adsorption of NLS on 304 stainless steel particles was directly measured. NLS adsorbs significantly on 304 stainless steel with maximum adsorption density close to bilayer coverage. Electrophoretic mobility data for 304 stainless steel particles show that the surface of 304 stainless steel is negative in NaCl solution at neutral pH. The adsorption of NLS makes the interfacial charge even more negative. The relationship between pitting inhibition and adsorption density of NLS suggests that NLS does not adsorb preferentially on the pit nucleation sites and complete inhibition requires that the whole surface be covered completely by NLS. The inhibition mechanism of NLS is proposed to be due mainly to the blocking effect of a negatively charged NLS adsorption layer. This study shows that in addition to the adsorption amount of surfactant, interfacial charge also plays an important role in pitting inhibition.

  19. Responsive organometallic polymer grafts: electrochemical switching of surface properties and current mediation behavior.

    Science.gov (United States)

    Song, Jing; Vancso, G Julius

    2011-06-07

    Quantitative adherence and friction measurements between atomic force microscopy (AFM) tips and reversibly oxidized and reduced poly(ferrocenyl dimethylsilane) (PFDMS) molecular layers grafted to Au are reported. Poly(ferrocenylsilanes) (PFSs) such as PFDMS owe their redox responsiveness to the presence of ferrocene units, bridged by substituted silicon units, in the main chain. Polymers were obtained by anionic polymerization, which allowed us to copolymerize sulfur containing end groups that facilitated grafting to Au surfaces. Electrochemical atomic force microscopy (ECAFM) was used to study adherence and friction as a function of the oxidation state of the polymer. Measurements of interfacial friction as a function of applied load on the nanoscale using Si(3)N(4) AFM tips revealed a reversible increase of the friction coefficient and adherence strength of the PFDMS layers with increasing oxidation state in NaClO(4) electrolytes. The variation of the electrolyte salts (NaClO(4) or NaNO(3)) allowed an assessment of surface counterion adsorption effects. Issues related to the interpretation of observed friction and adherence changes such as electrolyte anion-ferrocenium ion pair effects, and electrostatic forces due to tip surface charges are discussed. Unidirectional current flow was detected in cyclic voltammograms of the PFDMS layers in NaClO(4). This electrode rectification behavior could in principle be utilized for applications in thin film devices based on PFS films.

  20. 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.

  1. Electrochemical and ion transport characterisation of a nanoporous carbon derived from SiC

    OpenAIRE

    Zuleta, Marcelo

    2005-01-01

    In this doctoral project, a relatively new form of carbon material, with unique narrow pore size distribution around 7 Å and with uniform structure, has been electrochemically characterised using the single particle microelectrode technique. The carbon has been used as electrode material for supercapacitors. This type of capacitors is used as high power energy buffers in hybrid vehicles and for stationary power backup. The principle for the microelectrode technique consists of connecting a ca...

  2. 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

  3. Improvement of electrochemical activity of LiMnPO4-based cathode by surface iron enrichment

    Science.gov (United States)

    Xu, Xiaoyue; Wang, Tao; Bi, Yujing; Liu, Meng; Yang, Wenchao; Peng, Zhe; Wang, Deyu

    2017-02-01

    LiMnPO4 has attracted massive interests due to its appropriate redox potential and the success of its iron comparative in the lithium ion batteries. The bulk substitution has been widely used to address the poor electrochemical activity of LiMnPO4, which is much lower than that of LiFePO4. In this work, we compare the performance of the core-shell structure and the homogeneous substitution with the same Mn/Fe molar ratio of LiMn0.8Fe0.2PO4. The core-shell phosphate material after carbon coating is composed of a core part of quasi-single LiMnPO4 phase, and a 3-4 nm shell layer of quasi-single LiFePO4-phase, separated by the phase boundary with 1-2 nm thickness. It is interesting to reveal that the core-shell samples exhibit capacities of 156.4, 144.5, 128.2 mAh g-1 under 0.1C, 1C and 5C respectively, which are 5-10% higher than that of the homogenous substituted LiMn0.8Fe0.2PO4 at the corresponding rates, while both of these samples present excellent cyclic stability, still retaining ∼95% of the initial capacities after 1000 cycles under 1C discharging rate. Our results demonstrate that the main reason for LiMnPO4's poor electrochemical activity should be emphasized on the surface polarization, whereas the tardiness on bulk transportation is not as serious as it was presumed.

  4. Electrochemical Detection of Hydrogen Peroxide by Inhibiting the p-Benzenediboronic Acid-Triggered Assembly of Citrate-Capped Au/Ag Nanoparticles on Electrode Surface

    Directory of Open Access Journals (Sweden)

    Lin Liu

    2017-01-01

    Full Text Available Metal nanoparticles (NPs possess unique physicochemical attributes for creating effective recognition and transduction processes in chem/bio-sensing. In this work, we suggested that citrate-capped Au/Ag NPs could be used as the reporters for the design of hydrogen peroxide (H2O2 sensors with a simple manipulation principle and an easy detection procedure. Specifically, p-benzenediboronic acid (BDBA induced the aggregation of citrate-capped Au NPs through the cross-linking reaction between citrate and boronic acid of BDBA in solution. By modifying the electrode with a boronic acid derivative, the BDBA-induced assembly of Au NPs was achieved on the electrode surface. This led to a significant decrease in the electron transfer resistance due to the unique conductive ability of Au NPs. However, when the boronate group on the electrode surface was oxidized into its phenol format, the assembly of Au NPs on the electrode surface was not achieved. As a result, a higher electron transfer resistance was observed. The process could be monitored by electrochemical impedance technique. Furthermore, when Ag NPs were used instead of Au NPs in this design, the H2O2 concentration could be determined by measuring the linear-sweep voltammetry (LSV current through the solid-state Ag/AgCl reaction of Ag NPs. The results indicated that NP-based colorimetric assays could be developed into more sensitive electrochemical analysis.

  5. Deriving Albedo from Coupled MERIS and MODIS Surface Products

    Science.gov (United States)

    Gao, Feng; Schaaf, Crystal; Jin, Yu-Fang; Lucht, Wolfgang; Strahler, Alan

    2004-01-01

    MERIS Level 2 surface reflectance products are now available to the scientific community. This paper demonstrates the production of MERIS-derived surface albedo and Nadir Bidirectional Reflectance Distribution Function (BRDF) adjusted reflectances by coupling the MERIS data with MODIS BRDF products. Initial efforts rely on the specification of surface anisotropy as provided by the global MODIS BRDF product for a first guess of the shape of the BRDF and then make use all of the coincidently available, partially atmospherically corrected, cloud cleared, MERIS observations to generate MERIS-derived BRDF and surface albedo quantities for each location. Comparisons between MODIS (aerosol-corrected) and MERIS (not-yet aerosol-corrected) surface values from April and May 2003 are also presented for case studies in Spain and California as well as preliminary comparisons with field data from the Devil's Rock Surfrad/BSRN site.

  6. Electrochemical & osteoblast adhesion study of engineered TiO{sub 2} nanotubular surfaces on titanium alloys

    Energy Technology Data Exchange (ETDEWEB)

    Rahman, Zia Ur [School of Engineering and Technology, Central Michigan University, Mt. Pleasant, MI (United States); Haider, Waseem, E-mail: haide1w@cmich.edu [School of Engineering and Technology, Central Michigan University, Mt. Pleasant, MI (United States); Pompa, Luis [Department of Mechanical Engineering, University of Texas–Pan American, Edinburg, TX (United States); Deen, K.M. [Department of Metallurgy & Materials Engineering, CEET, University of the Punjab, 54590 Lahore (Pakistan); Department of Materials Engineering, University of British Columbia, Vancouver, BC V6T 1Z4 (Canada)

    2016-01-01

    TiO{sub 2} nanotubes were grafted on the surface of cpTi, Ti6Al4V and Ti6Al4V-ELI with the aim to provide a new podium for human pre-osteoblast cell (MC3T3) adhesion and proliferation. The surface morphology and chemistry of these alloys were examined with scanning electron microscopy and energy dispersive x-ray spectroscopy. TiO{sub 2} nanotubes were further characterized by cyclic potentiodynamic polarization tests and electrochemical impedance spectroscopy. The vertically aligned nanotubes were subjected to pre-osteoblast cell proliferation in order to better understand cell–material interaction. The study demonstrated that these cells interact differently with nanotubes of different titanium alloys. The significant acceleration in the growth rate of pre-osteoblast cell adhesion and proliferation is also witnessed. Additionally, the cytotoxicity of the leached metal ions was evaluated by using a tetrazolium-based bio-assay, MTS. Each group of data was operated for p < 0.05, concluded one way ANOVA to investigate the significance difference. - Highlights: • TiO{sub 2} nanotubes were grafted on cpTi, Ti6Al4V and Ti6Al4V-ELI via anodization. • MC3T3 cells interact differently with nanotubes of different titanium alloys. • TiO{sub 2} nanotubes have a positive impact on the osteoblast cell viability.

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

    Science.gov (United States)

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

    2016-10-01

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

  8. Surface Redox Chemistry of Immobilized Nanodiamond: Effects of Particle Size and Electrochemical Environment

    Science.gov (United States)

    Gupta, S.; McDonald, B.; Carrizosa, S. B.

    2017-07-01

    The size of the diamond particle is tailored to nanoscale (nanodiamond, ND), and the ND surface is engineered targeting specific (electrochemical and biological) applications. In this work, we investigated the complex surface redox chemistry of immobilized ND layer on conductive boron-doped diamond electrode with a broad experimental parameter space such as particle size (nano versus micron), scan rate, pH (cationic/acidic versus anionic/basic), electrolyte KCl concentration (four orders of magnitude), and redox agents (neutral and ionic). We reported on the significant enhancement of ionic currents while recording reversible oxidation of neutral ferrocene methanol (FcMeOH) by almost one order of magnitude than traditional potassium ferricyanide (K3Fe(CN)6) redox agent. The current enhancement is inversely related to ND particle diameter in the following order: 1 μm graphene (graphene oxide; GO and reduced GO). The findings are discussed in terms of interplay of sp 3-bonded C (ND core) and sp 2-bonded C (ND shell and graphene-based systems).

  9. Effect of Surface Pretreatment on Quality and Electrochemical Corrosion Properties of Manganese Phosphate on S355J2 HSLA Steel

    Directory of Open Access Journals (Sweden)

    Filip Pastorek

    2016-10-01

    Full Text Available High strength low alloy (HSLA steels exhibit many outstanding properties for industrial applications but suffer from unsatisfactory corrosion resistance in the presence of aggressive chlorides. Phosphate coatings are widely used on the surface of steels to improve their corrosion properties. This paper evaluates the effect of a manganese phosphate coating prepared after various mechanical surface treatments on the electrochemical corrosion characteristics of S355J2 steel in 0.1 M NaCl electrolyte simulating aggressive sea atmosphere. The manganese phosphate coating was created in a solution containing H3PO4, MnO2, dissolved low carbon steel wool, and demineralised H2O. Scanning electron microscopy (SEM was used for surface morphology observation supported by energy-dispersive X-ray analysis (EDX. The electrochemical corrosion characteristics were assessed by electrochemical impedance spectroscopy (EIS and potentiodynamic polarization (PD measurements in the solution of 0.1 M NaCl. Method of equivalent circuits and Tafel-extrapolation were used for the analysis of the obtained results. Performed experiments and analysis showed that the morphological and corrosion properties of the surface with manganese phosphate are negatively influenced by sandblasting surface pretreatment.

  10. Preparation and application of a novel electrochemical sensing material based on surface chemistry of polyhydroquinone

    Energy Technology Data Exchange (ETDEWEB)

    Dang, Xueping [Key Laboratory of Analytical Chemistry for Biology and Medicine (Ministry of Education), College of Chemistry and Molecular Sciences, Wuhan University, Wuhan 430072 (China); Hubei Collaborative Innovation Center for Advanced Organic Chemical Materials, Ministry of Education Key Laboratory for the Synthesis and Application of Organic Functional Molecules and College of Chemistry and Chemical Engineering, Hubei University, Wuhan 430062 (China); State Key Laboratory of Transducer Technology, Chinese Academy of Sciences, Beijing 10080 (China); Wang, Yingkai [Key Laboratory of Analytical Chemistry for Biology and Medicine (Ministry of Education), College of Chemistry and Molecular Sciences, Wuhan University, Wuhan 430072 (China); Hu, Chengguo, E-mail: cghu@whu.edu.cn [Key Laboratory of Analytical Chemistry for Biology and Medicine (Ministry of Education), College of Chemistry and Molecular Sciences, Wuhan University, Wuhan 430072 (China); State Key Laboratory of Transducer Technology, Chinese Academy of Sciences, Beijing 10080 (China); Huang, Jianlin; Chen, Huaixia; Wang, Shengfu [Hubei Collaborative Innovation Center for Advanced Organic Chemical Materials, Ministry of Education Key Laboratory for the Synthesis and Application of Organic Functional Molecules and College of Chemistry and Chemical Engineering, Hubei University, Wuhan 430062 (China); Hu, Shengshui, E-mail: sshu@whu.edu.cn [Key Laboratory of Analytical Chemistry for Biology and Medicine (Ministry of Education), College of Chemistry and Molecular Sciences, Wuhan University, Wuhan 430072 (China); State Key Laboratory of Transducer Technology, Chinese Academy of Sciences, Beijing 10080 (China)

    2014-07-01

    A new analogue of polydopamine (PDA), i.e., polyhydroquinone (PH{sub 2}Q), was polymerized and its surface chemistry was studied by different ways of characterization. PH{sub 2}Q was produced by the self-polymerization of H{sub 2}Q mediated by dissolved oxygen, and the self-polymerization process was strongly dependent on the type and the pH value of the buffer solutions. PH{sub 2}Q can not only achieve surface hydrophilization of different substrates like polyethylene terephthalate (PET) film, graphite strip, C{sub 12}SH/Au and wax slice, but also possess several unique properties like reversible adsorption, good solubility and low cost. These properties made PH{sub 2}Q an ideal polymeric modifier for the noncovalent functionalization of some nanomaterials. By simply grinding with PH{sub 2}Q, pristine multi-walled carbon nanotubes (MWNTs) can be readily dispersed in water with high solubility and good stability. The resulting MWNT–PH{sub 2}Q composite exhibited excellent electrochemical performance, which was employed for the simultaneous determination of dopamine (DA) and uric acid (UA). - Highlights: • Polyhydroquinone (PH{sub 2}Q) was produced by the self-polymerization of hydroquinone (H{sub 2}Q) mediated by dissolved oxygen. • PH{sub 2}Q can achieve surface hydrophilization of a variety of substrates. • PH{sub 2}Q is an ideal polymeric modifier for the functionalization of multi-walled carbon nanotubes (MWNTs). • The MWNT–PH{sub 2}Q composite can be employed for the simultaneous determination of dopamine (DA) and uric acid (UA)

  11. The Effects of Different Electrode Types for Obtaining Surface Machining Shape on Shape Memory Alloy Using Electrochemical Machining

    Science.gov (United States)

    Choi, S. G.; Kim, S. H.; Choi, W. K.; Moon, G. C.; Lee, E. S.

    2017-06-01

    Shape memory alloy (SMA) is important material used for the medicine and aerospace industry due to its characteristics called the shape memory effect, which involves the recovery of deformed alloy to its original state through the application of temperature or stress. Consumers in modern society demand stability in parts. Electrochemical machining is one of the methods for obtained these stabilities in parts requirements. These parts of shape memory alloy require fine patterns in some applications. In order to machine a fine pattern, the electrochemical machining method is suitable. For precision electrochemical machining using different shape electrodes, the current density should be controlled precisely. And electrode shape is required for precise electrochemical machining. It is possible to obtain precise square holes on the SMA if the insulation layer controlled the unnecessary current between electrode and workpiece. If it is adjusting the unnecessary current to obtain the desired shape, it will be a great contribution to the medical industry and the aerospace industry. It is possible to process a desired shape to the shape memory alloy by micro controlling the unnecessary current. In case of the square electrode without insulation layer, it derives inexact square holes due to the unnecessary current. The results using the insulated electrode in only side show precise square holes. The removal rate improved in case of insulated electrode than others because insulation layer concentrate the applied current to the machining zone.

  12. An investigation of the electrochemical action of the epoxy zinc-rich coatings containing surface modified aluminum nanoparticle

    Energy Technology Data Exchange (ETDEWEB)

    Jalili, M. [Nanomaterials and Nanocoatings Department, Institute for Color Science and Technology (ICST), PO 16765-654, Tehran (Iran, Islamic Republic of); Surface Coatings and Corrosion Department, Institute for Color Science and Technology (ICST), PO 16765-654, Tehran (Iran, Islamic Republic of); Rostami, M. [Nanomaterials and Nanocoatings Department, Institute for Color Science and Technology (ICST), PO 16765-654, Tehran (Iran, Islamic Republic of); Ramezanzadeh, B., E-mail: ramezanzadeh-bh@icrc.ac.ir [Surface Coatings and Corrosion Department, Institute for Color Science and Technology (ICST), PO 16765-654, Tehran (Iran, Islamic Republic of)

    2015-02-15

    Highlights: • Aluminum nanoparticle was modified with amino trimethylene phosphonic acid. • 2 wt% of zinc dust in zinc-rich paint was substituted by aluminum nanoparticles. • Surface modified aluminum nanoparticle improved the cathodic period of protection. • Aluminum nanoparticles enhanced the corrosion protection of the zinc-rich coating. - Abstract: Aluminum nanoparticle was modified with amino trimethylene phosphonic acid (ATMP). The surface characterization of the nanoparticles was done by X-ray photo electron spectroscopy (XPS), Fourier transform infrared spectroscopy (FTIR) and thermal gravimetric analysis. The influence of the replacement of 2 wt% of zinc dust in the standard zinc-rich epoxy coating by nanoparticles on the electrochemical action of the coating was studied by electrochemical impedance spectroscopy (EIS) and salt spray tests. The morphology and phase composition of the zinc rich paints were evaluated by X-ray diffraction (XRD) and filed-emission scanning electron microscopy (FE-SEM). Results showed that the ATMP molecules successfully adsorbed on the surface of Al nanoparticles. Results obtained from salt spray and electrochemical measurements revealed that the addition of surface modified nanoparticles to the zinc rich coating enhanced its galvanic action and corrosion protection properties.

  13. Surface-Enhanced Infrared Absorption of o-Nitroaniline on Nickel Nanoparticles Synthesized by Electrochemical Deposition

    Directory of Open Access Journals (Sweden)

    Yufang Niu

    2014-01-01

    Full Text Available Nickel nanoparticles were electrochemically deposited on indium-tin oxide (ITO coated glass plate in a modified Watt’s electrolyte. The surface-enhanced infrared absorption (SEIRA effect of the nanoparticles was evaluated by attenuated total reflection spectroscopy (ATR-FTIR using o-nitroaniline as a probe molecule. Electrodeposition parameters such as deposition time, pH value, and the type of surfactants were investigated. The morphology and the microstructure of the deposits were characterized by the field emission scanning electron microscope (FESEM and the atomic force microscope (AFM, respectively. The results indicate that the optimum parameters were potential of 1.3 V, time of 30 s, and pH of 8.92 in the solution of 0.3756 mol/L diethanolamine, 0.1 mol/L nickel sulfate, 0.01 mol/L nickel chloride, and 0.05 mol/L boric acid. The FESEM observation shows that the morphology of nickel nanoparticles with best enhancement effect is spherical and narrowly distributed particles with the average size of 50 nm. SEIRA enhancement factor is about 68.

  14. Influence of surface acoustic waves induced acoustic streaming on the kinetics of electrochemical reactions

    Science.gov (United States)

    Tietze, Sabrina; Schlemmer, Josefine; Lindner, Gerhard

    2013-12-01

    The kinetics of electrochemical reactions is controlled by diffusion processes of charge carriers across a boundary layer between the electrode and the electrolyte, which result in a shielding of the electric field inside the electrolyte and a concentration gradient across this boundary layer. In accumulators the diffusion rate determines the rather long time needed for charging, which is a major drawback for electric mobility. This diffusion boundary can be removed by acoustic streaming in the electrolyte induced by surface acoustic waves propagating of the electrode, which results in an increase of the charging current and thus in a reduction of the time needed for charging. For a quantitative study of the influence of acoustic streaming on the charge transport an electropolishing cell with vertically oriented copper electrodes and diluted H3PO4-Propanol electrolytes were used. Lamb waves with various excitation frequencies were exited on the anode with different piezoelectric transducers, which induced acoustic streaming in the overlaying electrolytic liquid. An increase of the polishing current of up to approximately 100 % has been obtained with such a set-up.

  15. High Surface Area Antimony-Doped Tin Oxide Electrodes Templated by Graft Copolymerization. Applications in Electrochemical and Photoelectrochemical Catalysis

    Energy Technology Data Exchange (ETDEWEB)

    Luo, Hanlin; Fang, Zhen; Song, Na; Garvey, Timothy; Lopez, Rene; Meyer, Thomas J.

    2015-11-18

    Mesoporous ATO nanocrystalline electrodes of micrometer thicknesses have been prepared from ATO nanocrystals and the grafted copolymer templating agents poly vinyl chloride-g-poly(oxyethylene methacrylate). As-obtained electrodes have high interfacial surface areas, large pore volumes, and rapid intraoxide electron transfer. The resulting high surface area materials are useful substrates for electrochemically catalyzed water oxidation. With thin added shells of TiO2 deposited by atomic layer deposition (ALD) and a surface-bound Ru(II) polypyridyl chromophore, they become photoanodes for hydrogen generation in the presence of a reductive scavenger.

  16. Photogeneration of singlet oxygen by the phenothiazine derivatives covalently bound to the surface-modified glassy carbon

    Energy Technology Data Exchange (ETDEWEB)

    Blacha-Grzechnik, Agata, E-mail: agata.blacha@polsl.pl [Faculty of Chemistry, Silesian University of Technology, Strzody 9, 44-100 Gliwice (Poland); Piwowar, Katarzyna; Krukiewicz, Katarzyna [Faculty of Chemistry, Silesian University of Technology, Strzody 9, 44-100 Gliwice (Poland); Koscielniak, Piotr; Szuber, Jacek [Institute of Electronics, Silesian University of Technology, Akademicka 16, 44-100 Gliwice (Poland); Zak, Jerzy K. [Faculty of Chemistry, Silesian University of Technology, Strzody 9, 44-100 Gliwice (Poland)

    2016-05-15

    Highlights: • The selected group of four NH{sub 2}-derivatives of phenothiazine was grafted to Glassy Carbon (GC) surface. • The grafted phenothiazines are able to generate {sup 1}O{sub 2} when activated by the radiation. • Such modified solid surfaces may find their application in the wastewater treatment. - Abstract: The selected group of four amine-derivatives of phenothiazine was covalently grafted to the glassy carbon surface in the four-step procedure consisting of the electrochemical reduction of the diazonium salt followed by the electrochemical and chemical post-modification steps. The proposed strategy involves the bonding of linker molecule to which the photosensitizer is attached. The synthesized organic layers were characterized by means of cyclic voltammetry, XPS and Raman Spectroscopy. It was shown that the phenothiazines immobilized via proposed strategy retain their photochemical properties and are able to generate {sup 1}O{sub 2} when activated by the laser radiation. The effectiveness of in situ singlet oxygen generation by those new solid photoactive materials was determined by means of UVVis spectroscopy. The reported, covalently modified solid surfaces may find their application as the singlet oxygen photogenerators in the fine chemicals’ synthesis or in the wastewater treatment.

  17. Computational and electrochemical investigation for corrosion inhibition of nickel in molar sulfuric acid by dihydrazide derivatives. Part II

    Directory of Open Access Journals (Sweden)

    H. Shokry

    2017-05-01

    Full Text Available Correlation of the efficiency of some dihydrazide derivatives, namely malonic acid (MAD, succinic acid (SAD and adipic acid (AAD dihydrazide, against the corrosion of nickel in 1 M sulfuric acid solution is discussed using electrochemical polarization method and quantum chemical calculations based on the ab initio method. The quantum chemical parameters calculated are, the highest occupied molecular orbital (HOMO, the lowest unoccupied molecular orbital (LUMO, the gap energy (ΔE, the dipole moment (μ, the softness (σ and the total energy (TE. The relations between the inhibition efficiency and some quantum parameters are discussed and correlations are proposed. The protection efficiencies of these compounds showed a certain relationship to Mulliken atomic charges and Fukui indices. Dihydrazide inhibitor (AAD exhibited the highest inhibition efficiency.

  18. Adsorption of antimicrobial indolicidin-derived peptides on hydrophobic surfaces.

    Science.gov (United States)

    Tsai, Ching-Wei; Ruaan, Ruoh-Chyu; Liu, Chih-I

    2012-07-17

    The hydrophobic interaction between antimicrobial peptides and membrane hydrophobic cores is usually related to their cytotoxicity. In this study, the adsorption mechanism of five plasma membrane-associated peptides, indolicidin (IL) and its four derivatives, with hydrophobic ligands was investigated to understand the relationship between peptide hydrophobicity and bioactivity. The hydrophobic adsorption mechanisms of IL and its derivatives were interpreted thermodynamically and kinetically by reversed-phase chromatography (RPC) analysis and surface plasmon resonance (SPR) measurement, respectively. IL and its derivatives possess a similar random coil structure in both aqueous and organic solvents. Thermodynamic analysis showed that the binding enthalpy of peptides with higher electropositivity was lower than those with lower electropositivity and exhibited unfavorable binding entropy. Higher electropositivity peptides adsorbed to the hydrophobic surface arising from the less bound solvent on the peptide surface. A comparison with the kinetic analysis showed that IL and its derivatives adopt a two-state binding model (i.e., adsorption onto and self-association on the hydrophobic acyl chain) to associate with the hydrophobic surface, and the binding affinity of peptide self-association correlates well with peptide hemolysis. Consequently, this study provided a novel concept for understanding the action of plasma membrane-associated peptides.

  19. COUPLING OF LIPOPOLYSACCHARIDE-DERIVED CARBOHYDRATES ONTO SOLID SURFACES

    DEFF Research Database (Denmark)

    2000-01-01

    The present invention provides a method for immobilising a polysaccharide (PS) to a solid surface, said polysaccharide having a keto-carboxy group (-C(=O)-COOH) or a ketal or hemiketal group corresponding thereto, e.g. derived from KDO (2-keto-3-deoxy-D-mannooctonic acid), the method comprising t...

  20. 2D zirconium-based metal-organic framework nanosheets for highly sensitive detection of mucin 1: consistency between electrochemical and surface plasmon resonance methods

    Science.gov (United States)

    He, Linghao; Duan, Fenghe; Song, Yingpan; Guo, Chuanpan; Zhao, Hui; Tian, Jia-Yue; Zhang, Zhihong; Liu, Chun-Sen; Zhang, Xiaojing; Wang, Peiyuan; Du, Miao; Fang, Shao-Ming

    2017-06-01

    Two-dimensional (2D) zirconium-based metal-organic framework (denoted as 521-MOF) nanosheets with the thickness of 6.0-7.5 nm were prepared with the aid of polyvinyl pyrrolidone (PVP) under the mild conditions and low temperature (50 °C). Since 521-MOF nanosheets displayed good electrochemical activity, high surface area, and strong affinity interaction between the MOF and the oligonucleotides sequences, they can impel the immobilization of large amounts of aptamer strands when applied as a platform of biosensor. As a result, the developed aptasensor exhibited sensitive bio-recognition for the cancer determination marker protein, mucin 1 (MUC1). The combination of electrochemical techniques and surface plasmon resonance spectroscopy (SPR) was performed to probe the kinetic processes of the aptamer immobilization and the MUC1 detection. The consistency between different determination approaches was observed, in which the developed aptasensor based on 521-MOF nanosheets exhibits pretty high sensitivity for detecting MUC1 with a low detect limit of 0.12 and 0.65 pg·ml-1 deduced from electrochemical impedance spectroscopy and SPR, respectively, within the broad concentration range of MUC1 from 0.001 to 0.5 ng·ml-1. Simultaneously, a comparable affinity constant, K a, was derived from EIS and SPR, which also demonstrates that this new biosensing strategy has high selectivity, stability, reproducibility, and good applicability for the MUC1 detection in the human serum. The present finding indicates that the synthesized 521-MOF nanosheets can be employed in the fields of the biosensing or biomedical diagnosis and explored for different kinds of biosensors.

  1. Topographic and Electrochemical Ti6Al4V Alloy Surface Characterization in Dry and Wet Reciprocating Sliding

    Directory of Open Access Journals (Sweden)

    Z. Doni

    2013-09-01

    Full Text Available This present paper shows the behavior of functional integrity of the state Ti6Al4V alloy under reciprocating sliding wear conditions in acomparative way for two different counter materials, steel and ceramicballs in dry and corrosive environment (3.5% NaCl. The surface integrity analysis of the dry reciprocating wear tests was based on the evolution of The roughness parameters with the applied load. In the case of reciprocating wear tests in corrosive environment the surface integrity analysis was based on electrochemical parameters. Comparative analysis of the evolution of the roughness parameters with the applied load shows a higher stability of the Ti6Al4V/Al2O3 contact pair, while from the point of view of the electrochemical parameters the Tribological properties are worse than Ti6Al4V/steel ball contact pair.

  2. Electrochemical Surface Potential due to Classical Point Charge Models Drives Anion Adsorption to the Air-Water Interface

    Energy Technology Data Exchange (ETDEWEB)

    Baer, Marcel D.; Stern, Abraham C.; Levin, Yan; Tobias, Douglas J.; Mundy, Christopher J.

    2012-06-07

    Herein, we present research that suggests that the underlying physics that drive simple empirical models of anions (e.g. point charge, no polarization) to the air-water interface, with water described by SPC/E, or related partial charge models is different than when both ions and water are modeled with quantum mechanical based interactions. Specifically, we will show that the driving force of ions to the air-water interface for point charge models results from both cavitation and the negative electrochemical surface potential. We will demonstrate that we can fully characterize the role of the free energy due to the electrochemical surface potential computed from simple empirical models and its role in ionic adsorption within the context of dielectric continuum theory (DCT). Our research suggests that a significant part of the electrochemical surface potential in empirical models appears to be an artifact of the failure of point charge models in the vicinity of a broken symmetry. This work was supported by the U.S. Department of Energy‘s (DOE) Office of Basic Energy Sciences, Division of Chemical Sciences, Geosciences and Biosciences. Pacific Northwest National Laboratory (PNNL) is operated for the Department of Energy by Battelle.

  3. Investigation of Electrochemical Behaviour of Quercetin on the Modified Electrode Surfaces with Procaine and Aminophenyl in Non-Aquous Medium

    Directory of Open Access Journals (Sweden)

    Ibrahim Ender Mulazimoglu

    2008-01-01

    Full Text Available In this study, cyclic voltammetry and electrochemical ımpedance spectroscopy have been used to investigate the electrochemical behaviour of quercetin (3,3′,4′,5,7-pentahydroxyflavone on the procaine and aminophenyl modified electrode. The modification of procaine and aminophenyl binded electrode surface with quercetin was performed in +0,3/+2,8 V (for procaine and +0,4/+1,5 V (for aminophenyl potential range using 100 mV s-1 scanning rate having 10 cycle. A solution of 0.1 M tetrabutylammonium tetrafluoroborate in acetonitrile was used as a non-aquous solvent. For the modification process a solution of 1 mM quercetin in 0.1 M tetrabutylammonium tetrafluoroborate was used. In order to obtain these two surface, a solution of 1 mM procaine and 1 mM nitrophenyl diazonium salt in 0.1 M tetrabutylammonium tetrafluoroborate was used. By using these solutions bare glassy carbon electrode surface was modified. Nitrophenyl was reduced to amine group in 0.1 M HCl medium on the nitrophenyl modified glassy carbon elelctrode surface. Procaine modified glassy carbon electrode surface was quite electroactive. Although nitrophenyl modified glassy carbon elelctrode surface was electroinactive, it was activated by reducing nitro group into amine group. For the characterization of the modified surface 1 mM ferrocene in 0.1 M tetrabutylammonium tetrafluoroborate for cyclic voltammetry and 1 mM ferricyanide/ferrocyanide (1:1 mixture in 0,1 M KCl for electrochemical impedance spectroscopy were used.

  4. Electrochemical control of peptide self-organization on atomically flat solid surfaces: A Case study with Graphite.

    Science.gov (United States)

    Seki, Takakazu; So, Christopher R; Page, Tamon R; Starkebaum, David Alan; Hayamizu, Yuhei; Sarikaya, Mehmet

    2017-10-02

    Nanoscale self-organization of biomolecules, such as proteins and peptides, on solid surfaces under controlled conditions is an important issue to establish functional bio/solid soft interfaces for bioassays, biosensors, and biofuel cells. Electrostatic interaction between proteins and surfaces is one of the most essential parameters in the adsorption and self-assembly of proteins on solid surfaces. Although the adsorption of proteins has been studied with respect to the electrochemical surface potential, the self-assembly of proteins or peptides forming well-organized nanostructures templated by lattice structure of the solid surfaces has not been studied in the relation with the surface potential. In this work, we utilize graphite-binding peptides (GrBPs) selected by phage display method to investigate the relationship between the electrochemical potential of the highly ordered pyrolytic graphite (HOPG) and peptide self-organization forming long-range ordered structures. Under modulated electrical bias, graphite-binding peptides form various ordered structures, such as well-ordered nanowires, dendritic structures, wavy wires, amorphous (disordered) structures, and islands. Systematic investigation of the correlation between peptide sequence and self-organizational characteristics reveals that the presence of the bias-sensitive amino acid modules in the peptide sequence has a significant effect on not only surface coverage, but also the morphological features of self-assembled structures. Our results show a new method to control peptide self-assembly by means of applied electrochemical bias, as well as peptide design-rules for construction of functional soft bio/solid interfaces that could be integrated in a wide range of practical implementations.

  5. Electrochemical, interfacial, and surface studies of the conversion of carbon dioxide to liquid fuels on tin electrodes

    Science.gov (United States)

    Wu, Jingjie

    maximize the triple phase boundary length for simultaneous high current density and selectivity towards formate formation (Chapter 3). The Sn GDEs was incorporated into a home-designed scalable full electrochemical cell which features a buffer layer of circulating liquid electrolyte mediating the proton concentration at cathode electrode surface. The Sn GDEs exhibited excellent short-term performance for CO2 reduction with high selectivity towards formate formation at low overpotentials in the full electrochemical cell. Additionally, coupling water oxidation and CO2 reduction was demonstrated in this full electrochemical cell to mimic biosynthesis (Chapter 4). The rapid degradation of selectivity towards formate formation on Sn GDEs in the full electrochemical cell, however, was observed during long-term operation. The degradation mechanism was unraveled due to the decrease of electrode potential resulted from substantial increase of internal ohmic resistance of the full electrochemical cell. The unexpected rise of internal ohmic resistance was attributed to the pulverization of 100 nm Sn nanoparticles due to the hydrogen diffusion induced stress. Based on the understanding of the origin of Sn nanoparticles pulverization, SnO2 nanoparticles of 3˜3.5 nm close to the critical size were utilized and reduced in situ to form Sn catalyst for electrochemical reduction of CO2. The pulverization was suppressed and subsequently a stable performance of electrodes was obtained (Chapter 5). Due to the affinity to oxygen, Sn nanoparticle surface is covered by a native thin oxide layer. The performance of Sn GDEs towards CO2 reduction strongly depends on the initial thickness of the surface oxide layer. The selectivity towards formate production dropped while the hydrogen yield increased as the initial thickness of the oxide layer increased (Chapter 6). These results suggest the underlying of surface structure on the selectivity of Sn electrode for CO2 reduction and provide insight into

  6. Popcorn-Derived Porous Carbon Flakes with an Ultrahigh Specific Surface Area for Superior Performance Supercapacitors.

    Science.gov (United States)

    Hou, Jianhua; Jiang, Kun; Wei, Rui; Tahir, Muhammad; Wu, Xiaoge; Shen, Ming; Wang, Xiaozhi; Cao, Chuanbao

    2017-09-13

    Popcorn-derived porous carbon flakes have been successfully fabricated from the biomass of maize. Utilizing the "puffing effect", the nubby maize grain turned into materials with an interconnected honeycomb-like porous structure composed of carbon flakes. The following chemical activation method enabled the as-prepared products to possess optimized porous structures for electrochemical energy-storage devices, such as multilayer flake-like structures, ultrahigh specific surface area (SBET: 3301 m2 g-1), and a high content of micropores (microporous surface area of 95%, especially the optimized sub-nanopores with the size of 0.69 nm) that can increase the specific capacitance. The as-obtained sample displayed excellent specific capacitance of 286 F g-1 at 90 A g-1 for supercapacitors. Moreover, the unique porous structure demonstrated an ideal way to improve the volumetric energy density performance. A high energy density of 103 Wh kg-1 or 53 Wh L-1 has been obtained in the case of ionic liquid electrolyte, which is the highest among reported biomass-derived carbon materials and will satisfy the urgent requirements of a primary power source for electric vehicles. This work may prove to be a fast, green, and large-scale synthesis route by using the large nubby granular materials to synthesize applicable porous carbons in energy-storage devices.

  7. Electrochemical Impedance Spectroscopy and Potentiodynamic Polarization Analysis on Anticorrosive Activity of Thiophene-2-Carbaldehyde Derivative in Acid Medium

    Directory of Open Access Journals (Sweden)

    Nimmy Kuriakose

    2014-01-01

    Full Text Available The corrosion inhibition efficiency of thiophene-2-carbaldehyde tryptophan (T2CTRY on mild steel (MS in 1 M HCl solution has been investigated and compared using weight loss measurements, electrochemical impedance spectroscopy, and potentiodynamic polarization analysis. The Schiff base exhibited very good corrosion inhibition on mild steel in HCl medium and the inhibition efficiency increased with the increase in concentration of the inhibitor. The adsorption of the inhibitor on the surface of the corroding metal obeys Freundlich isotherm. Thermodynamic parameters (Kads, ΔG ads0 were calculated using adsorption isotherm. Polarization studies revealed that T2CTRY acts as a mixed type inhibitor. A maximum of 96.2% inhibition efficiency was achieved by EIS studies at a concentration of 1 mM.

  8. Electrochemical nanocomposite-derived sensor for the analysis of chemical oxygen demand in urban wastewaters.

    Science.gov (United States)

    Gutiérrez-Capitán, Manuel; Baldi, Antoni; Gómez, Raquel; García, Virginia; Jiménez-Jorquera, Cecilia; Fernández-Sánchez, César

    2015-02-17

    This work reports on the fabrication and comparative analytical assessment of electrochemical sensors applied to the rapid analysis of chemical oxygen demand (COD) in urban waste waters. These devices incorporate a carbon nanotube-polystyrene composite, containing different inorganic electrocatalysts, namely, Ni, NiCu alloy, CoO, and CuO/AgO nanoparticles. The sensor responses were initially evaluated using glucose as standard analyte and then by analyzing a set of real samples from urban wastewater treatment plants. The estimated COD values in the samples were compared with those provided by an accredited laboratory using the standard dichromate method. The sensor prepared with the CuO/AgO-based nanocomposite showed the best analytical performance. The recorded COD values of both the sensor and the standard method were overlapped, considering the 95% confidence intervals. In order to show the feasible application of this approach for the detection of COD online and in continuous mode, the CuO/AgO-based nanocomposite sensor was integrated in a compact flow system and applied to the detection of wastewater samples, showing again a good agreement with the values provided by the dichromate method.

  9. The electrochemical oxidation of salicylic acid and its derivatives on modified PbO2-electrodes

    Directory of Open Access Journals (Sweden)

    Olesia B. Shmychkova

    2017-11-01

    Full Text Available The results of the study of electrochemical oxidation of salicylic acid on PbO2-based anodes for effective wastewater treatment from organic pollutants have been summarized. Both the influence of various factors on the decomposition rate of organic substances and the influence of various modifying additives of lead dioxide anode on the process of mineralization of salicylic acid have been established. The total probable sequence of reactions to salicylic acid mineralization has been proposed. It is established that the destruction of salicylic acid in the first stage occurs through the accumulation of aromatic hydroxylation products, and during the total destruction - the destruction of the aromatic system with the formation of aliphatic compounds takes place. It is shown that the use of PbO2, deposited from methanesulfonate electrolytes and modified electrodes significantly reduces the conversion time of salicylic acid in aliphatic products compared to lead dioxide anodes obtained by traditional technology from nitrate bath. The highest degradation rate occurs at the anodes modified by bismuth. It was found that the destruction of the 5-aminosalicylic acid occurs through an intermediate oxidation of amino-group to hydroxy.

  10. Electrochemical synthesis of novel {pi}-extended phenoxazine derivatives of porphyrincatecholes

    Energy Technology Data Exchange (ETDEWEB)

    Osati, Samira; Davarani, Saied Saeed Hosseiny [Department of Chemistry, Faculty of Science, Shahid Beheshti University, G.C, Evin, 1983963113 Tehran (Iran, Islamic Republic of); Safari, Nasser, E-mail: n-safari@cc.sbu.ac.ir [Department of Chemistry, Faculty of Science, Shahid Beheshti University, G.C, Evin, 1983963113 Tehran (Iran, Islamic Republic of); Banitaba, Mohammad Hossein [Department of Chemistry, Faculty of Science, Shahid Beheshti University, G.C, Evin, 1983963113 Tehran (Iran, Islamic Republic of)

    2011-10-30

    Three new functionalized phenoxazine-catechol porphyrins 7a-c have been synthesized by a green one-pot method and structurally characterized by spectroscopic analysis. The electro-oxidation of 5,10,15,20-tetrakis(2,3-dihydroxyphenyl) porphyrins(1a-c) with four catechol units in the presence of 2-aminophenol 8 as bidentate nucleophile has been done and phenoxazine rings have been formed by intermolecular and intramolecular Michael addition reactions. Spectroscopic characterization and voltammetry results have allowed us to propose four independent ECEC mechanisms for the electrochemical oxidation pathway. The functionalization of the porphyrins affected their photophysical properties. Expansion of the UV-vis spectrum range and the decrease of the fluorescence intensity of the products would support the energy transfer between the porphyrin core excited states to the four substitutions as the electron acceptor subunits. SEM images indicate that this method produces regularly shaped manganese porphyrin nano-particles 7c that possess a cubic nano structure.

  11. ESR and electrochemical study of 5-nitroindazole derivatives with antiprotozoal activity.

    Science.gov (United States)

    Olea-Azar, Claudio; Cerecetto, Hugo; Gerpe, Alejandra; González, Mercedes; Arán, Vicente J; Rigol, Carolina; Opazo, Lucía

    2006-01-01

    The electrochemistry of 3-alkoxy- and 3-hydroxy-1-[omega-(dialkylamino)alkyl]-5-nitroindazole derivatives were characterized using cyclic voltammetry in DMSO. The nitro reduction process was studied and this was affected by the acid moieties present in these compounds. A nitro anion self-protonation process was observed. This phenomenon was studied by cyclic voltammetry in presence of increasing amount of NaOH. The reactivity of the nitro anion radical of these derivatives with glutathione was also studied by cyclic voltammetry. The oxidizing effect of glutathione is supported by the parallel decrease of the anodic peak current and increase of the cathodic peak in the cyclic voltammograms, corresponding to the wave of the nitro anion radical from uncharged species with the addition of glutathione. Nitro anion radicals obtained by electrolytic reduction of these derivatives were measured and analyzed in DMSO using electron spin resonance spectroscopy.

  12. Electrochemical Coupling of Biomass-Derived Acids: New C8Platforms for Renewable Polymers and Fuels.

    Science.gov (United States)

    Wu, Linglin; Mascal, Mark; Farmer, Thomas J; Arnaud, Sacha Pérocheau; Wong Chang, Maria-Angelica

    2017-01-10

    Electrolysis of biomass-derived carbonyl compounds is an alternative to condensation chemistry for supplying products with chain length >C 6 for biofuels and renewable materials production. Kolbe coupling of biomass-derived levulinic acid is used to obtain 2,7-octanedione, a new platform molecule only two low process-intensity steps removed from raw biomass. Hydrogenation to 2,7-octanediol provides a chiral secondary diol largely unknown to polymer chemistry, whereas intramolecular aldol condensation followed by hydrogenation yields branched cycloalkanes suitable for use as high-octane, cellulosic gasoline. Analogous electrolysis of an itaconic acid-derived methylsuccinic monoester yields a chiral 2,5-dimethyladipic acid diester, another underutilized monomer owing to lack of availability. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  13. Energy storage on ultrahigh surface area activated carbon fibers derived from PMIA.

    Science.gov (United States)

    Castro-Muñiz, Alberto; Suárez-García, Fabián; Martínez-Alonso, Amelia; Tascón, Juan M D; Kyotani, Takashi

    2013-08-01

    High-performance carbon materials for energy storage applications have been obtained by using poly(m-phenylene isophthalamide), PMIA, as a precursor through the chemical activation of the carbonized aramid fiber by using KOH. The yield of the process of activation was remarkably high (25-40 wt%), resulting in activated carbon fibers (ACFs) with ultrahigh surface areas, over 3000 m(2) g(-1) , and pore volumes exceeding 1.50 cm(3) g(-1) , keeping intact the fibrous morphology. The porous structure and the surface chemical properties could easily be controlled through the conditions of activation. The PMIA-derived ACFs were tested in two types of energy storage applications. At -196 °C and 1 bar, H2 uptake values of approximately 3 t% were obtained, which, in combination with the textural properties, rendered it a good candidate for H2 adsorption at high pressure and temperature. The performance of the ACFs as electrodes for electrochemical supercapacitors was also investigated. Specific capacitance values between 297 and 531 g(-1) at 50 mA g(-1) were obtained in aqueous electrolyte (1 H2 SO4 ), showing different behaviors depending on the surface chemical properties. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  14. Performance of nitrogen- and sulfur-containing carbon material derived from thiourea and formaldehyde as electrochemical capacitor

    Science.gov (United States)

    Tsubota, Toshiki; Takenaka, Kaori; Murakami, Naoya; Ohno, Teruhisa

    In order to investigate the performance of an electrochemical capacitor consisting of a nitrogen- and sulfur-containing carbon material, the carbon material derived from thiourea and urea was synthesized by a polymerization process of the urea resin. No solid appeared after the polymerization process. When the dried sample after the polymerization process was heated in flowing N2 gas, we obtained carbon material. However, there was no product when only thiourea was heated under the same conditions. The percentages of nitrogen and sulfur in all the samples synthesized from thiourea were roughly 5-20 wt.% and 3-8 wt.% even after washing with hot water, respectively. No specific peak derived from the redox reaction appeared in the CV graphs for the samples. The capacitance value of T-urea800W, which was synthesized by the heat treatment at 800 °C and then wash with hot water, was 138.8 F g -1 at the current density of 50 mA g -1 in a 1 M H 2SO 4 water solution whereas that value of a commercial activated carbon was 107.1 F g -1 under the same conditions. It was presumed from the XPS measurements that the status of the nitrogen and sulfur in the materials are a pyridine-like nitrogen at the edge part of the graphitic structure, a quaternary nitrogen in the graphitic-layered structure, and S 0, S 4+, and S 2-, respectively.

  15. Influence of sodium chloride and weak organic acids (flux residues) on electrochemical migration of tin on surface mount chip components

    DEFF Research Database (Denmark)

    Verdingovas, Vadimas; Jellesen, Morten Stendahl; Ambat, Rajan

    2013-01-01

    The electrolytic properties of sodium chloride and no-clean solder flux residue, and their effects on electrochemical migration and dendrite growth on surface mount chip capacitors were investigated. The leakage current dependency on concentration of contaminants was measured by a solution...... conductivity method and compared with current measurements using DC voltage. The effect of electrolyte concentration and potential bias on the probability of electrochemical migration was investigated using a water droplet method on chip capacitors. The results from leakage current and conductivity measurement...... showed a difference which is caused by polarization effects, and demonstrated existing issues when indexing contamination levels on printed circuit board assemblies using a standardised solvent extract method. The experimental results showed that dendrite growth was dependent on the type and amount...

  16. Electrochemical synthesis of elongated noble metal nanoparticles, such as nanowires and nanorods, on high-surface area carbon supports

    Science.gov (United States)

    Adzic, Radoslav; Blyznakov, Stoyan; Vukmirovic, Miomir

    2015-08-04

    Elongated noble-metal nanoparticles and methods for their manufacture are disclosed. The method involves the formation of a plurality of elongated noble-metal nanoparticles by electrochemical deposition of the noble metal on a high surface area carbon support, such as carbon nanoparticles. Prior to electrochemical deposition, the carbon support may be functionalized by oxidation, thus making the manufacturing process simple and cost-effective. The generated elongated nanoparticles are covalently bound to the carbon support and can be used directly in electrocatalysis. The process provides elongated noble-metal nanoparticles with high catalytic activities and improved durability in combination with high catalyst utilization since the nanoparticles are deposited and covalently bound to the carbon support in their final position and will not change in forming an electrode assembly.

  17. Improvement of the Electrochemical Behavior of Steel Surfaces Using a [Ti-Al/Ti-Al-N] n Multilayer System

    Science.gov (United States)

    Ipaz, L.; Aperador, W.; Caicedo, J. C.; Esteve, J.; Zambrano, G.

    2013-05-01

    The aim of this work is to improve the corrosion resistance of AISI D3 steel surfaces using a [Ti-Al/Ti-Al-N] n multilayer system deposited with different periods (Λ) and bilayer numbers ( n), via magnetron co-sputtering pulsed d.c. procedure, from a metallic (Ti-Al) binary target. The multilayer coatings were characterized by cross-sectional scanning electron microscopy that showed the modulation and microstructure of the [Ti-Al/Ti-Al-N] n multilayer system. The composition of the single Ti-Al and Ti-Al-N layer films was studied via x-ray photoelectron spectroscopy, where typical signals for Ti2p1/2, Ti2p, N1s, and Al2p3/2 were detected. The electrochemical properties were evaluated by electrochemical impedance spectroscopy and Tafel polarization curves. The optimal electrochemical behavior was obtained for the [Ti-Al/Ti-Al-N] n multilayered period of Λ = 25 nm (100 bilayers). At these conditions, the maximum polarization resistance (1719.32 kΩ cm2) and corrosion rate (0.7 μmy) were 300 and 35 times higher than that of uncoated AISI D3 steel substrate (5.61 kΩ cm2 and 25 μmy, respectively). Finally, scanning electron microscopy was used to analyze the [Ti-Al/Ti-Al-N] n multilayered surface after the corrosive attack. The improvement effects in the electrochemical behavior of the AISI D3 coated with the [Ti-Al/Ti-Al-N] n multilayered coatings could be attributed to the number of interfaces that act as obstacles for the inward and outward diffusions of Cl- ions, generating an increment in the energy or potential required for translating the corrosive ions across the coating/substrate interface.

  18. Influence of clinical use on physical-structural surface properties and electrochemical potential of NiTi endodontic instruments.

    Science.gov (United States)

    Pereira, E S J; Amaral, C C F; Gomes, J A C P; Peters, O A; Buono, V T L; Bahia, M G A

    2017-03-22

    To investigate the surface morphology and electrochemical potential of superelastic (SE), M-Wire (MW) and shape memory technology (SMT) NiTi instruments before and after single clinical use in vivo. A total of 60 ProTaper Universal F2 (PTU-SE), ProTaper Next X2 (PTN-MW), Typhoon (TYP), Hyflex (HF) and Vortex Blue (VB), the last three SMT, and size 25, .06 taper (n = 6 of each type) files were examined. Scanning electron microscopy (SEM), X-ray energy-dispersive spectroscopy (EDS) and electrochemical potential analysis were employed before and after clinical use. Statistical analysis was performed with one-way analysis of variance and Bonferroni's post hoc test. Significance was determined at the 95% confidence level for both tests. SEM observations of new instruments indicated the presence of marks left by the machining process during manufacturing and EDS revealed the existence of an oxide coating on shape memory instruments. After clinical use, the five types were associated with propagation of transverse cracks 3 mm from the tip. The surface oxide layer of TYP, HF and VB instruments had microcracks in multiple directions, whilst TYP and HF had fragmentation in chip form of the oxide layer. EDS analysis demonstrated a significant reduction of the oxide layer in shape memory instruments, except for VB. Electrochemical potentials were higher for shape memory instruments than for M-Wire and superelastic NiTi instruments, respectively (P < 0.05). It appears that shape memory technology NiTi instruments have a dysfunctional oxide layer after clinical use. Additionally, they featured higher electrochemical potential relative to NiTi instruments manufactured from M-Wire, and conventional superelastic NiTi alloy. © 2017 International Endodontic Journal. Published by John Wiley & Sons Ltd.

  19. The anodic stripping voltammetry of nanoparticles: electrochemical evidence for the surface agglomeration of silver nanoparticles

    Science.gov (United States)

    Toh, Her Shuang; Batchelor-McAuley, Christopher; Tschulik, Kristina; Uhlemann, Margitta; Crossley, Alison; Compton, Richard G.

    2013-05-01

    Analytical expressions for the anodic stripping voltammetry of metallic nanoparticles from an electrode are provided. First, for reversible electron transfer, two limits are studied: that of diffusionally independent nanoparticles and the regime where the diffusion layers originating from each particle overlap strongly. Second, an analytical expression for the voltammetric response under conditions of irreversible electron transfer kinetics is also derived. These equations demonstrate how the peak potential for the stripping process is expected to occur at values negative of the formal potential for the redox process in which the surface immobilised nanoparticles are oxidised to the corresponding metal cation in the solution phase. This work is further developed by considering the surface energies of the nanoparticles and its effect on the formal potential for the oxidation. The change in the formal potential is modelled in accordance with the equations provided by Plieth [J. Phys. Chem., 1982, 86, 3166-3170]. The new analytical expressions are used to investigate the stripping of silver nanoparticles from a glassy carbon electrode. The relative invariance of the stripping peak potential at low surface coverages of silver is shown to be directly related to the surface agglomeration of the nanoparticles.

  20. Novel redox species polyaniline derivative-Au/Pt as sensing platform for label-free electrochemical immunoassay of carbohydrate antigen 199

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Liyuan; Shan, Jiao; Feng, Feng; Ma, Zhanfang, E-mail: mazhanfang@cnu.edu.cn

    2016-03-10

    A novel electrochemical redox-active nanocomposite was synthesized by a one-pot method using N,N′-diphenyl-p-phenylediamine as monomer, and HAuCl{sub 4} and K{sub 2}PtCl{sub 4} as co-oxidizing agents. The as-prepared poly(N,N′-diphenyl-p-phenylediamine)-Au/Pt exhibited admirable electrochemical redox activity at 0.15 V, excellent H{sub 2}O{sub 2} electrocatalytic ability and favorable electron transfer ability. Based on these, the evaluation of the composite as sensing substrate for label-free electrochemical immunosensing to the sensitive detection of carbohydrate antigen 199 was described. This technique proved to be a prospective detection tool with a wide liner range from 0.001 U mL{sup −1} to 40 U mL{sup −1}, and a low detection limit of 2.3 × 10{sup −4} U mL{sup −1} (S/N = 3). In addition, this method was used for the analysis of human serum sample, and good agreement was obtained between the values and those of enzyme-linked immunosorbent assay, implying the potential application in clinical research. Importantly, the strategy of the present substrate could be extended to other polymer-based nanocomposites such as polypyrrole derivatives or polythiophene derivatives, and this could be of great significance for the electrochemical immunoassay. - Highlights: • A novel electrochemical redox composite PPPD-Au/Pt was synthesized by one-pot method. • PPPD-Au/Pt was used as sensing substrate for label-free electrochemical immunosensor. • The immunosensor showed wide detection range and ultralow detection limit for the detection of CA199.

  1. The Influence of Electrolytic Concentration on the Electrochemical Deposition of Calcium Phosphate Coating on a Direct Laser Metal Forming Surface

    Directory of Open Access Journals (Sweden)

    Qianyue Sun

    2017-01-01

    Full Text Available A calcium phosphate (CaP coating on titanium surface enhances its biocompatibility, thus facilitating osteoconduction and osteoinduction with the inorganic phase of the human bone. Electrochemical deposition has been suggested as an effective means of fabricating CaP coatings on porous surface. The purpose of this study was to develop CaP coatings on a direct laser metal forming implant using electrochemical deposition and to investigate the effect of electrolytic concentration on the coating’s morphology and structure by X-ray diffraction, scanning electron microscopy, water contact angle analysis, and Fourier transform infrared spectroscopy. In group 10−2, coatings were rich in dicalcium phosphate, characterized to be thick, layered, and disordered plates. In contrast, in groups 10−3 and 10−4, the relatively thin and well-ordered coatings predominantly consisted of granular hydroxyapatite. Further, the hydrophilicity and cell affinity were improved as electrolytic concentration increased. In particular, the cells cultured in group 10−3 appeared to have spindle morphology with thick pseudopodia on CaP coatings; these spindles and pseudopodia strongly adhered to the rough and porous surface. By analyzing and evaluating the surface properties, we provided further knowledge on the electrolytic concentration effect, which will be critical for improving CaP coated Ti implants in the future.

  2. Synthesis, spectroscopic characterization, electrochemical behaviour and thermal decomposition studies of some transition metal complexes with an azo derivative

    Science.gov (United States)

    Sujamol, M. S.; Athira, C. J.; Sindhu, Y.; Mohanan, K.

    2010-01-01

    Complexes of manganese(II), cobalt(II), nickel(II), copper(II) and zinc(II) with a novel heterocyclic azo derivative, formed by coupling diazotized 2-amino-3-carbethoxy-4,5-dimethylthiophene with acetylacetone were synthesized and characterized on the basis of elemental analyses, molar conductance, magnetic susceptibility measurements, UV-vis, IR, 1H NMR and EPR spectral data. Spectral studies revealed that the ligand existed in an internally hydrogen bonded azo-enol form rather than the keto-hydrazone form and coordinated to the metal ion in a tridentate fashion. Analytical data revealed that all the complexes exhibited 1:1 metal-ligand ratio. On the basis of electronic spectral data and magnetic susceptibility measurements, suitable geometry was proposed for each complex. The nickel(II) complex has undergone facile transesterification reaction when refluxed in methanol for a long period. The ligand and the copper(II) complex were subjected to X-ray diffraction study. The electrochemical behaviour of copper(II) complex was investigated by cyclic voltammetry. The thermal behaviour of the same complex was also examined by thermogravimetry.

  3. Stability of Residual Oxides in Oxide-Derived Copper Catalysts for Electrochemical CO2 Reduction Investigated with 18 O Labeling.

    Science.gov (United States)

    Lum, Yanwei; Ager, Joel W

    2018-01-08

    Oxide-derived (OD) Cu catalysts have high selectivity towards the formation of multi-carbon products (C2 /C3 ) for aqueous electrochemical CO2 reduction (CO2 R). It has been proposed that a large fraction of the initial oxide can be surprisingly resistant to reduction, and these residual oxides play a crucial catalytic role. The stability of residual oxides was investigated by synthesizing 18 O-enriched OD Cu catalysts and testing them for CO2 R. These catalysts maintain a high selectivity towards C2 /C3 products (ca. 60 %) for up to 5 h in 0.1 m KHCO3 at -1.0 V vs. RHE. However, secondary-ion mass spectrometry measurements show that only a small fraction (CO2 R. Furthermore, we show that OD Cu can reoxidize rapidly, which could compromise the accuracy of ex situ methods for determining the true oxygen content. © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  4. 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.

  5. Effect of hydrodynamics and surface roughness on the electrochemical behaviour of carbon steel in CSG produced water

    Energy Technology Data Exchange (ETDEWEB)

    Eyu, Gaius Debi; Will, Geoffrey, E-mail: g.will@qut.edu.au; Dekkers, Willem; MacLeod, Jennifer

    2015-12-01

    Highlights: • Surface roughness increases the anodic current density under dynamic conditions. • Pitting corrosion increases with an increasing surface roughness for carbon steel in coal seam gas produced water. • Flow accelerates the mass transfer of the corrosion product under dynamic conditions. • Corrosion rate of carbon steel decreased with immersion time. - Abstract: The influence of fluid flow, surface roughness and immersion time on the electrochemical behaviour of carbon steel in coal seam gas produced water under static and hydrodynamic conditions has been studied. The disc electrode surface morphology before and after the corrosion test was characterized using scanning electron microscopy (SEM). The corrosion product was examined using X-ray photoelectron spectroscopy (XPS) and X-ray diffractometry (XRD).The results show that the anodic current density increased with increasing surface roughness and consequently a decrease in corrosion surface resistance. Under dynamic flow conditions, the corrosion rate increased with increasing rotating speed due to the high mass transfer coefficient and formation of non-protective akaganeite β-FeO(OH) and goethite α-FeO(OH) corrosion scale at the electrode surface. The corrosion rate was lowest at 0 rpm. The corrosion rate decreased in both static and dynamic conditions with increasing immersion time. The decrease in corrosion rate is attributed to the deposition of corrosion products on the electrode surface. SEM results revealed that the rougher surface exhibited a great tendency toward pitting corrosion.

  6. An electrochemical and surface analysis study of the influence of phosphorus on the corrosion of iron in calcium nitrate

    Energy Technology Data Exchange (ETDEWEB)

    Windisch, C.F. Jr.; Baer, D.R.; Jones, R.H.; Engelhard, M.H.

    1990-10-01

    Intergranular stress corrosion cracking (IGSCC) of metallic alloys including iron is strongly influenced by the presence of grain boundary impurities such as phosphorus. In this study to determine how phosphorus affects the corrosion of iron, electrochemical polarization methods were used in conjunction with surface analyses employing ultra-high vacuum transfer. Specifically, these methods were used to examine the corrosion of iron, iron/phosphorus alloys, and iron implanted with phosphorus in deaerated 55 wt % Ca(NO{sub 3}){sub 2} solutions at 60{degree}C. 18 refs., 13 figs., 1 tab.

  7. Sulfur-doped nanoporous carbon spheres with ultrahigh specific surface area and high electrochemical activity for supercapacitor

    Science.gov (United States)

    Liu, Simin; Cai, Yijin; Zhao, Xiao; Liang, Yeru; Zheng, Mingtao; Hu, Hang; Dong, Hanwu; Jiang, Sanping; Liu, Yingliang; Xiao, Yong

    2017-08-01

    Development of facile and scalable synthesis process for the fabrication of nanoporous carbon materials with large specific surface areas, well-defined nanostructure, and high electrochemical activity is critical for the high performance energy storage applications. The key issue is the dedicated balance between the ultrahigh surface area and highly porous but interconnected nanostructure. Here, we demonstrate the fabrication of new sulfur doped nanoporous carbon sphere (S-NCS) with the ultrahigh surface area up to 3357 m2 g-1 via a high-temperature hydrothermal carbonization and subsequent KOH activation process. The as-prepared S-NCS which integrates the advantages of ultrahigh porous structure, well-defined nanospherical and modification of heteroatom displays excellent electrochemical performance. The best performance is obtained on S-NCS prepared by the hydrothermal carbonization of sublimed sulfur and glucose, S-NCS-4, reaching a high specific capacitance (405 F g-1 at a current density of 0.5 A g-1) and outstanding cycle stability. Moreover, the symmetric supercapacitor is assembled by S-NCS-4 displays a superior energy density of 53.5 Wh kg-1 at the power density of 74.2 W kg-1 in 1.0 M LiPF6 EC/DEC. The synthesis method is simple and scalable, providing a new route to prepare highly porous and heteroatom-doped nanoporous carbon spheres for high performance energy storage applications.

  8. 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.

    2017-11-01

    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.

  9. 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.

  10. Pomelo peels-derived porous activated carbon microsheets dual-doped with nitrogen and phosphorus for high performance electrochemical capacitors

    Science.gov (United States)

    Wang, Zhen; Tan, Yongtao; Yang, Yunlong; Zhao, Xiaoning; Liu, Ying; Niu, Lengyuan; Tichnell, Brandon; Kong, Lingbin; Kang, Long; Liu, Zhen; Ran, Fen

    2018-02-01

    In this work, biomass pomelo peel is used to fabricate the porous activated carbon microsheets, and diammonium hydrogen phosphate (DHP) is employed to dual-dope carbon with nitrogen and phosphorus elements. With the benefit of DHP inducement and dual-doping of nitrogen and phosphorus, the prepared carbon material has a higher carbon yield, and exhibits higher specific surface area (about 807.7 m2/g), and larger pore volume (about 0.4378 cm3/g) with hierarchically structure of interconnected thin microsheets compared to the pristine carbon. The material exhibits not only high specific capacitance (240 F/g at 0.5 A/g), but also superior cycling performance (approximately 100% of capacitance retention after 10,000 cycles at 2 A/g) in 2 M KOH aqueous electrolyte. Furthermore, the assembled symmetric electrochemical capacitor in 1 M Na2SO4 aqueous electrolyte exhibits a high energy density of 11.7 Wh/kg at a power density of 160 W/kg.

  11. Electroendocytosis is driven by the binding of electrochemically produced protons to the cell's surface.

    Directory of Open Access Journals (Sweden)

    Nadav Ben-Dov

    Full Text Available Electroendocytosis involves the exposure of cells to pulsed low electric field and is emerging as a complementary method to electroporation for the incorporation of macromolecules into cells. The present study explores the underlying mechanism of electroendocytosis and its dependence on electrochemical byproducts formed at the electrode interface. Cell suspensions were exposed to pulsed low electric field in a partitioned device where cells are spatially restricted relative to the electrodes. The cellular uptake of dextran-FITC was analyzed by flow cytometery and visualized by confocal microscopy. We first show that uptake occurs only in cells adjacent to the anode. The enhanced uptake near the anode is found to depend on electric current density rather than on electric field strength, in the range of 5 to 65 V/cm. Electrochemically produced oxidative species that impose intracellular oxidative stress, do not play any role in the stimulated uptake. An inverse dependence is found between electrically induced uptake and the solution's buffer capacity. Electroendocytosis can be mimicked by chemically acidifying the extracellular solution which promotes the enhanced uptake of dextran polymers and the uptake of plasmid DNA. Electrochemical production of protons at the anode interface is responsible for inducing uptake of macromolecules into cells exposed to a pulsed low electric field. Expanding the understanding of the mechanism involved in electric fields induced drug-delivery into cells, is expected to contribute to clinical therapy applications in the future.

  12. Electrochemical modification of chromium surfaces using 4-nitro- and4-fluorobenzenediazonium salts

    DEFF Research Database (Denmark)

    Hinge, Mogens; Cecatto, Marcel; Kingshott, Peter

    2009-01-01

    Chromium surfaces can be electrografted with organic surface films using 4-nitro- or 4-fluorobenzenediazonium salts, despite the fact that the surfaces are covered with a protective chromium oxide layer......Chromium surfaces can be electrografted with organic surface films using 4-nitro- or 4-fluorobenzenediazonium salts, despite the fact that the surfaces are covered with a protective chromium oxide layer...

  13. Enhancement of electrochemical discharge machining accuracy and surface integrity using side-insulated tool electrode with diamond coating

    Science.gov (United States)

    Tang, Weidong; Kang, Xiaoming; Zhao, Wansheng

    2017-06-01

    Electrochemical discharge machining (ECDM) is an emerging non-traditional processing technology used to machine electrical non-conductive material like glass and ceramics, by using the electrochemical discharge phenomena around the tool electrode. In the general ECDM drilling process, the gas film forms and electrical discharge appears at both the tool end and the tool sidewall that were exposed to the electrolyte. The undesirable sidewall discharge enlarges the hole entrance diameter and destroys the hole surface integrity. In order to prevent the sidewall discharge, a side-insulated tool electrode with a 4 μm-thick diamond coating layer was used in ECDM micro-hole drilling. The gas film formation and electrical discharge mostly happened on the tool end due to the insulation layer on the tool sidewall. Experiments showed that, compared with the traditional tool electrode, the side-insulated tool electrode achieves a smaller hole diameter and better surface integrity without an obvious heat affected zone at the hole entrance. Furthermore, the hole diameter nearly remains the same as the machining depth increases from 50 μm to 500 μm. The side-insulated electrode has an advantage in enhancing shape accuracy by reducing the taper angle of the micro hole. When the machining depth is 600 μm, the side-insulated electrode achieves a much smaller hole taper angle ({{3.3}\\circ} ) than the traditional tool electrode does ({{6.4}\\circ} ).

  14. A Study of the Mechanism of the Hydrogen Evolution Reaction on Nickel by Surface Interrogation Scanning Electrochemical Microscopy.

    Science.gov (United States)

    Liang, Zhenxing; Ahn, Hyun S; Bard, Allen J

    2017-04-05

    The hydrogen evolution reaction (HER) on Ni in alkaline media was investigated by scanning electrochemical microscopy under two operating modes. First, the substrate generation/tip collection mode was employed to extract the "true" cathodic current associated with the HER from the total current in the polarization curve. Compared to metallic Ni, the electrocatalytic activity of the HER is improved in the presence of the low-valence-state oxide of Ni. This result is in agreement with a previous claim that the dissociative adsorption of water can be enhanced at the Ni/Ni oxide interface. Second, the surface-interrogation scanning electrochemical microscopy (SI-SECM) mode was used to directly measure the coverage of the adsorbed hydrogen on Ni at given potentials. Simulation indicates that the hydrogen coverage follows a Frumkin isotherm with respect to the applied potential. On the basis of the combined analysis of the Tafel slope and surface hydrogen coverage, the rate-determining step is suggested to be the adsorption of hydrogen (Volmer step) in the investigated potential window.

  15. Interactions of doxorubicin with self-assembled monolayer-modified electrodes: electrochemical, surface plasmon resonance (SPR), and gravimetric studies.

    Science.gov (United States)

    Nieciecka, Dorota; Krysinski, Pawel

    2011-02-01

    We present the results on the partitioning of doxorubicin (DOX), a potent anticancer drug, through the model membrane system, self-assembled monolayers (SAMs) on gold electrodes. The monolayers were formed from alkanethiols of comparable length with different ω-terminal groups facing the aqueous electrolyte: the hydrophobic -CH(3) groups for the case of dodecanethiol SAMs or hydrophilic -OH groups of mercaptoundecanol SAMs. The electrochemical experiments combined with the surface plasmon resonance (SPR) and gravimetric studies show that doxorubicin is likely adsorbed onto the surface of hydrophilic monolayer, while for the case of the hydrophobic one the drug mostly penetrates the monolayer moiety. The adsorption of the drug hinders further penetration of doxorubicin into the monolayer moiety.

  16. Polycyclic ferrocenyl(dihydro)thiazepine derivatives: Diastereo-selective synthesis, characterization, electrochemical behavior, theoretical and biological investigation.

    Science.gov (United States)

    Sánchez García, Jessica J; Toledano-Magaña, Yanis; Flores-Alamo, Marcos; Martínez-Klimova, Elena; Galindo-Murillo, Rodrigo; Hernández-Ayala, Luis F; Ortiz-Frade, Luis; García-Ramos, Juan C; Klimova, Elena I

    2017-01-01

    The reaction of E-2-ferrocenylmethylidenetetralones and E,E-2,6-bis-(ferrocenylmethylidene)-cyclohexanone with 2-aminothiophenol proceed with high diastereoselectivity, forming the ~4.5:1 mixture of trans- and cis-isomers of polycyclic ferrocenylthiazepines, respectively. The reactions of E,E-2,5-bis-(ferrocenylmethylidene)cyclopentanone and E,E-3,5-bis-(ferrocenylmethylidene)-1-methyl-4-piperidone with 2-aminothiophenol take place stereo specifically to form the diastereomeric tricyclic thiazepines of cis- and trans-configuration, respectively. The structures of the obtained compounds were established by IR, (1)H and (13)C NMR spectroscopy and mass-spectrometry. The structures of the trans-tetralino[1,2a]-, trans-5,7-dimethyltetralino[1,2a]-2-ferrocenyl [1,5]benzo-2,3-dihydrothiazepines and cis-5-ferrocenyl-methylidenecyclopentano[1,2a]-2-ferrocenyl- [1,5]benzo-2,3-dihydrothiazepine were confirmed by X-ray diffraction analysis. An electrochemical study reveals that the diferrocenyl derivatives belong to a Class I compounds of the Robin-Day classification. This behavior is explained by the analysis of frontier orbitals as calculated by density functional theory, showing that only one ferrocenyl unit participates in the generation of HOMO and LUMO orbitals. Compounds 4a and 4c showed similar capacity to inhibit the proliferation of HM1: IMSS trophozoite cultures than the first choice drug for human amoebiasis treatment, metronidazole. Morphological changes induced in the trophozoites after drug exposure suggest a redox in balance as the probable mechanism of the parasite death. Copyright © 2016 Elsevier Inc. All rights reserved.

  17. 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

  18. Synthesis, Characterization, Electrochemical and Surface Morphologies of Polyazomethines Containing Silane and Phosphazene Units.

    Science.gov (United States)

    Temizkan, Kevser; Kaya, İsmet

    2017-05-17

    Polyazomethines containing silane and phosphazene groups were synthesized via elimination reactions of dihydroxy compounds containing imine bonding with phosphazane and silane dichloride. The structures of monomers and polymers containing phosphazane and silane groups were supported by (1)H-NMR, (13)C-NMR, FT-IR and UV-Vis techniques. Electrochemical properties of the prepared Schiff bases and polymers were given by cyclic voltammetric (CV) analysis. Thermal properties of synthesized monomers and polymers were determined by TG-DTA and TG-DTA, DMA and DSC techniques, respectively. Molecular mass distributions of polymers are determined with gel permeation chromatography (GPC) measurement. Morphologic images of polymers containing heteroatom (silane/phosphazene) and azomethine linkage in the main chain were investigated by SEM techniques. The electrochemical band gap values of SB-1, SB-2, P-1, P-2 and P-3 compounds were found as 3.09, 3.30, 2.63, 3.07 and 3.04 eV, respectively.

  19. Ultrasound-enhanced electrochemical mineralization of perfluorooctanoic acid in aqueous solutions: Assessed by response surface methodology

    Directory of Open Access Journals (Sweden)

    Gholamreza Bonyadinejad

    2016-01-01

    Materials and Methods: The CCD was performed using three different variables such as current density (CD (mA/cm 2 , pH, and supporting electrolyte (EL concentration (mM. The total organic carbon (TOC removal was determined as an indicator of PFOA mineralization. A Shimadzu TOC analyzer was used to measure the TOC of the samples. The Ti/PbO 2 electrode was prepared using the electrochemical deposition method. In order to enhance the electrochemical mineralization, ultrasonic (US radiation was used. The US frequency was 20 kHz. Results: The optimum conditions for PFOA mineralization in synthetic solution were EL concentration of 94 mM, pH of 2, and CD of 83.64 mA/cm 2 , which resulted in complete TOC removal. The results indicated that the most effective factor for PFOA mineralization was CD. Besides, the TOC removal efficiency significantly increased with increasing CD. Conclusions: Under optimum conditions, the mineralization of PFOA was almost completed after 90 min of sonoelectrolysis. Therefore, sonoelectrolysis was found to be a more effective technique for mineralization of an environmentally persistent compound.

  20. Electrochemical surface science twenty years later: Expeditions into the electrocatalysis of reactions at the core of artificial photosynthesis

    Science.gov (United States)

    Soriaga, Manuel P.; Baricuatro, Jack H.; Cummins, Kyle D.; Kim, Youn-Geun; Saadi, Fadl H.; Sun, Guofeng; McCrory, Charles C. L.; McKone, James R.; Velazquez, Jesus M.; Ferrer, Ivonne M.; Carim, Azhar I.; Javier, Alnald; Chmielowiec, Brian; Lacy, David C.; Gregoire, John M.; Sanabria-Chinchilla, Jean; Amashukeli, Xenia; Royea, William J.; Brunschwig, Bruce S.; Hemminger, John C.; Lewis, Nathan S.; Stickney, John L.

    2015-01-01

    Surface science research fixated on phenomena and processes that transpire at the electrode-electrolyte interface has been pursued in the past. A considerable proportion of the earlier work was on materials and reactions pertinent to the operation of small-molecule fuel cells. The experimental approach integrated a handful of surface-sensitive physical-analytical methods with traditional electrochemical techniques, all harbored in a single environment-controlled electrochemistry-surface science apparatus (EC-SSA); the catalyst samples were typically precious noble metals constituted of well-defined single-crystal surfaces. More recently, attention has been diverted from fuel-to-energy generation to its converse, (solar) energy-to-fuel transformation; e.g., instead of water synthesis (from hydrogen and oxygen) in fuel cells, water decomposition (to hydrogen and oxygen) in artificial photosynthesis. The rigorous surface-science protocols remain unchanged but the experimental capabilities have been expanded by the addition of several characterization techniques, either as EC-SSA components or as stand-alone instruments. The present manuscript describes results selected from on-going studies of earth-abundant electrocatalysts for the reactions that underpin artificial photosynthesis: nickel-molybdenum alloys for the hydrogen evolution reaction, calcium birnessite as a heterogeneous analogue for the oxygen-evolving complex in natural photosynthesis, and single-crystalline copper in relation to the carbon dioxide reduction reaction.

  1. Pratt & Whitney ESCORT derivative for mars surface power

    Science.gov (United States)

    Feller, Gerald J.; Joyner, Russell

    1999-01-01

    The purpose of this paper is to address the applicability of a common reactor system design from the Pratt & Whitney ESCORT nuclear thermal rocket engine concept to support current NASA mars surface-based power requirements. The ESCORT is a bimodal engine capable of supporting a wide range of propulsive thermal and vehicle electrical power requirements. The ESCORT engine is powered by a fast-spectrum beryllium-reflected CERMET-fueled nuclear reactor. In addition to an expander cycle propulsive mode, the ESCORT is capable of operating in an electrical power mode. In this mode, the reactor is used to heat a mixture of helium and xenon to drive a closed-loop Brayton cycle in order to generate electrical energy. Recent Design Reference Mission requirements (DRM) from NASA Johnson Space Center and NASA Lewis Research Center studies in 1997 and 1998 have detailed upgraded requirements for potential mars transfer missions. The current NASA DRM requires a nuclear thermal propulsion system capable of delivering total mission requirements of 200170 N (45000 lbf) thrust and 50 kWe of spacecraft electrical power. Additionally, these requirements detailed a surface power system capable of providing approximately 160 kW of electrical energy over an approximate 10 year period within a given weight and volume envelope. Current NASA studies use a SP-100 reactor (0.8 MT) and a NERVA derivative (1.6 MT) as baseline systems. A mobile power cart of approximate dimensions 1.7 m×4.5 m×4.4 m has been conceptualized to transport the reactor power system on the Mars Surface. The 63.25 cm diameter and 80.25 cm height of the ESCORT and its 1.3 MT of weight fit well within the current weight and volume target range of the NASA DRM requirements. The modifications required to the ESCORT reactor system to support this upgraded electrical power requirements along with operation in the Martian atmospheric conditions are addressed in this paper. Sufficient excess reactivity and burnup capability

  2. Synthesis of trimethoprim metal complexes: Spectral, electrochemical, thermal, DNA-binding and surface morphology studies.

    Science.gov (United States)

    Demirezen, Nihat; Tarınç, Derya; Polat, Duygu; Ceşme, Mustafa; Gölcü, Ayşegül; Tümer, Mehmet

    2012-08-01

    Complexes of trimethoprim (TMP), with Cu(II), Zn(II), Pt(II), Ru(III) and Fe(III) have been synthesized. Then, these complexes have been characterized by spectroscopic techniques involving UV-vis, IR, mass and (1)H NMR. CHN elemental analysis, electrochemical and thermal behavior of complexes have also been investigated. The electrochemical properties of all complexes have been investigated by cyclic voltammetry (CV) using glassy carbon electrode. The biological activity of the complexes has been evaluated by examining their ability to bind to calf-thymus DNA (CT DNA) with UV spectroscopy and cyclic voltammetry. UV studies of the interaction of the complexes with DNA have shown that these compounds can bind to CT DNA. The binding constants of the complexes with CT DNA have also been calculated. The cyclic voltammograms of the complexes in the presence of CT DNA have shown that the complexes can bind to CT DNA by both the intercalative and the electrostatic binding mode. The antimicrobial activity of these complexes has been evaluated against three Gram-positive and four Gram-negative bacteria. Antifungal activity against two different fungi has been evaluated and compared with the reference drug TMP. Almost all types of complexes show excellent activity against all type of bacteria and fungi. The morphology of the CT DNA, TMP, metal ions and metal complexes has been investigated by scanning electron microscopy (SEM). To get the SEM images, the interaction of compounds with CT DNA has been studied by means of differential pulse voltammetry (DPV) at CT DNA modified pencil graphite electrode (PGE). The decrease in intensity of the guanine oxidation signals has been used as an indicator for the interaction mechanism. Copyright © 2012 Elsevier B.V. All rights reserved.

  3. Electrochemical micromachining of micro-dimple arrays on cylindrical inner surfaces using a dry-film photoresist

    Directory of Open Access Journals (Sweden)

    Qu Ningsong

    2014-08-01

    Full Text Available The application of surface textures has been employed to improve the tribological performance of various mechanical components. Various techniques have been used for the application of surface textures such as micro-dimple arrays, but the fabrication of such arrays on cylindrical inner surfaces remains a challenge. In this study, a dry-film photoresist is used as a mask during through-mask electrochemical micromachining to successfully prepare micro-dimple arrays with dimples 94 μm in diameter and 22.7 μm deep on cylindrical inner surfaces, with a machining time of 9 s and an applied voltage of 8 V. The versatility of this method is demonstrated, as are its potential low cost and high efficiency. It is also shown that for a fixed dimple depth, a smaller dimple diameter can be obtained using a combination of lower current density and longer machining time in a passivating sodium nitrate electrolyte.

  4. Engineering the Surface/Interface Structures of Titanium Dioxide Micro and Nano Architectures towards Environmental and Electrochemical Applications

    Directory of Open Access Journals (Sweden)

    Xiaoliang Wang

    2017-11-01

    Full Text Available Titanium dioxide (TiO2 materials have been intensively studied in the past years because of many varied applications. This mini review article focuses on TiO2 micro and nano architectures with the prevalent crystal structures (anatase, rutile, brookite, and TiO2(B, and summarizes the major advances in the surface and interface engineering and applications in environmental and electrochemical applications. We analyze the advantages of surface/interface engineered TiO2 micro and nano structures, and present the principles and growth mechanisms of TiO2 nanostructures via different strategies, with an emphasis on rational control of the surface and interface structures. We further discuss the applications of TiO2 micro and nano architectures in photocatalysis, lithium/sodium ion batteries, and Li–S batteries. Throughout the discussion, the relationship between the device performance and the surface/interface structures of TiO2 micro and nano structures will be highlighted. Then, we discuss the phase transitions of TiO2 nanostructures and possible strategies of improving the phase stability. The review concludes with a perspective on the current challenges and future research directions.

  5. Large-scale, Lithography-free Production of Transparent Nanostructured Surface for Dual-functional Electrochemical and SERS Sensing

    DEFF Research Database (Denmark)

    Sanger, Kuldeep; Durucan, Onur; Wu, Kaiyu

    2017-01-01

    -reversible behavior with decrease in peak potential separation (∆Ep ~90mV) and higher peak currents (Ipa/Ipc ~1), comparing to planar electrodes (∆Ep ~560mV). The oxidation potential of PAR was also lowered by ~80 mV on nanostructured electrodes. To illustrate dual-functional sensing, quantitative evaluation of PAR...... aspect ratios distributed homogeneously on a 4-inch fused silica wafer. The sensor was made up of three-electrode array, obtained by subsequent e-beam evaporation of Au on nanostructures in selected areas through a shadow mask. The SERS performance was evaluated through surface-averaged enhancement...... factor (EF), which was ~6.2 x 105, and spatial uniformity of EF, which was ~13% in terms of relative standard deviation. Excellent electrochemical performance and reproducibility were revealed by recording cyclic voltammograms. On nanostructured electrodes, paracetamol (PAR) showed an improved quasi...

  6. Electrochemical Oxidation of Resorcinol in Aqueous Medium Using Boron-Doped Diamond Anode: Reaction Kinetics and Process Optimization with Response Surface Methodology.

    Science.gov (United States)

    Körbahti, Bahadır K; Demirbüken, Pelin

    2017-01-01

    Electrochemical oxidation of resorcinol in aqueous medium using boron-doped diamond anode (BDD) was investigated in a batch electrochemical reactor in the presence of Na 2 SO 4 supporting electrolyte. The effect of process parameters such as resorcinol concentration (100-500 g/L), current density (2-10 mA/cm 2 ), Na 2 SO 4 concentration (0-20 g/L), and reaction temperature (25-45°C) was analyzed on electrochemical oxidation using response surface methodology (RSM). The optimum operating conditions were determined as 300 mg/L resorcinol concentration, 8 mA/cm 2 current density, 12 g/L Na 2 SO 4 concentration, and 34°C reaction temperature. One hundred percent of resorcinol removal and 89% COD removal were obtained in 120 min reaction time at response surface optimized conditions. These results confirmed that the electrochemical mineralization of resorcinol was successfully accomplished using BDD anode depending on the process conditions, however the formation of intermediates and by-products were further oxidized at much lower rate. The reaction kinetics were evaluated at optimum conditions and the reaction order of electrochemical oxidation of resorcinol in aqueous medium using BDD anode was determined as 1 based on COD concentration with the activation energy of 5.32 kJ/mol that was supported a diffusion-controlled reaction.

  7. Artificially-built solid electrolyte interphase via surface-bonded vinylene carbonate derivative on graphite by molecular layer deposition

    Science.gov (United States)

    Chae, Seulki; Lee, Jeong Beom; Lee, Jae Gil; Lee, Tae-jin; Soon, Jiyong; Ryu, Ji Heon; Lee, Jin Seok; Oh, Seung M.

    2017-12-01

    Vinylene carbonate (VC) is attached in a ring-opened form on a graphite surface by molecular layer deposition (MLD) method, and its role as a solid electrolyte interphase (SEI) former is studied. When VC is added into the electrolyte solution of a graphite/LiNi0.5Mn1.5O4 (LNMO) full-cell, it is reductively decomposed to form an effective SEI on the graphite electrode. However, VC in the electrolyte solution has serious adverse effects due to its poor stability against electrochemical oxidation on the LNMO positive electrode. A excessive acid generation as a result of VC oxidation is observed, causing metal dissolution from the LNMO electrode. The dissolved metal ions are plated on the graphite electrode to destroy the SEI layer, eventually causing serious capacity fading and poor Coulombic efficiency. The VC derivative on the graphite surface also forms an effective SEI layer on the graphite negative electrode via reductive decomposition. The detrimental effects on the LNMO positive electrode, however, can be avoided because the bonded VC derivative on the graphite surface cannot move to the LNMO electrode. Consequently, the graphite/LNMO full-cell fabricated with the VC-attached graphite outperforms the cells without VC or with VC in the electrolyte, in terms of Coulombic efficiency and capacity retention.

  8. Microscopically derived potential energy surfaces from mostly structural considerations

    Energy Technology Data Exchange (ETDEWEB)

    Ermamatov, M.J. [Instituto de Física, Universidade Federal Fluminense, 24210-340, Niterói, Rio de Janeiro (Brazil); Institute of Nuclear Physics, Ulughbek, Tashkent 100214 (Uzbekistan); Hess, Peter O., E-mail: hess@nucleares.unam.mx [Instituto de Ciencias Nucleares, UNAM, Circuito Exterior, C.U., A.P. 70-543, 04510, Mexico D.F. (Mexico)

    2016-08-15

    A simple procedure to estimate the quadrupole Potential-Energy-Surface (PES) is presented, using mainly structural information, namely the content of the shell model space and the Pauli exclusion principle. Further microscopic properties are implicitly contained through the use of results from the Möller and Nix tables or experimental information. A mapping to the geometric potential is performed yielding the PES. The General Collective Model is used in order to obtain an estimate on the spectrum and quadrupole transitions, adjusting only the mass parameter. First, we test the conjecture on known nuclei, deriving the PES and compare them to known data. We will see that the PES approximates very well the structure expected. Having acquired a certain confidence, we predict the PES of several chain of isotopes of heavy and super-heavy nuclei and at the end we investigate the structure of nuclei in the supposed island of stability. One of the main points to show is that simple assumptions can provide already important information on the structure of nuclei outside known regions and that spectra and electromagnetic transitions can be estimated without using involved calculations and assumptions. The procedure does not allow to calculate binding energies. The method presented can be viewed as a starting point for further improvements.

  9. Effects of Nanowire Length and Surface Roughness on the Electrochemical Sensor Properties of Nafion-Free, Vertically Aligned Pt Nanowire Array Electrodes

    Directory of Open Access Journals (Sweden)

    Zhiyang Li

    2015-09-01

    Full Text Available In this paper, vertically aligned Pt nanowire arrays (PtNWA with different lengths and surface roughnesses were fabricated and their electrochemical performance toward hydrogen peroxide (H2O2 detection was studied. The nanowire arrays were synthesized by electroplating Pt in nanopores of anodic aluminum oxide (AAO template. Different parameters, such as current density and deposition time, were precisely controlled to synthesize nanowires with different surface roughnesses and various lengths from 3 μm to 12 μm. The PtNWA electrodes showed better performance than the conventional electrodes modified by Pt nanowires randomly dispersed on the electrode surface. The results indicate that both the length and surface roughness can affect the sensing performance of vertically aligned Pt nanowire array electrodes. Generally, longer nanowires with rougher surfaces showed better electrochemical sensing performance. The 12 μm rough surface PtNWA presented the largest sensitivity (654 μA·mM−1·cm−2 among all the nanowires studied, and showed a limit of detection of 2.4 μM. The 12 μm rough surface PtNWA electrode also showed good anti-interference property from chemicals that are typically present in the biological samples such as ascorbic, uric acid, citric acid, and glucose. The sensing performance in real samples (river water was tested and good recovery was observed. These Nafion-free, vertically aligned Pt nanowires with surface roughness control show great promise as versatile electrochemical sensors and biosensors.

  10. A Review of Surface Analysis Techniques for the Investigation of the Phenomenon of Electrochemical Promotion of Catalysis with Alkaline Ionic Conductors

    Directory of Open Access Journals (Sweden)

    Jesús González-Cobos

    2016-01-01

    Full Text Available Electrochemical Promotion of Catalysis (EPOC with alkali ionic conductors has been widely studied in literature due to its operational advantages vs. alkali classical promotion. This phenomenon allows to electrochemically control the alkali promoter coverage on a catalyst surface in the course of the catalytic reaction. Along the study of this phenomenon, a large variety of in situ and ex situ surface analysis techniques have been used to investigate the origin and mechanism of this kind of promotion. In this review, we analyze the most important contributions made on this field which have clearly evidenced the presence of adsorbed alkali surface species on the catalyst films deposited on alkaline solid electrolyte materials during EPOC experiments. Hence, the use of different surface analysis techniques such as scanning electron microscopy (SEM, energy-dispersive X-ray spectroscopy (EDX, X-ray diffraction (XRD, X-ray photoelectron spectroscopy (XPS, scanning photoelectron microscopy (SPEM, or scanning tunneling microscopy (STM, led to a better understanding of the alkali promoting effect, and served to confirm the theory of electrochemical promotion on this kind of catalytic systems. Given the functional similarities between alkali electrochemical and chemical promotion, this review aims to bring closer this phenomenon to the catalysis scientific community.

  11. Corrosion performance of reinforced mortar in the presence of polymeric nano-aggregates : Electrochemical behavior, surface analysis, and properties of the steel/cement paste interface

    NARCIS (Netherlands)

    Hu, J.; Koleva, D.A.; Van Breugel, K.

    2012-01-01

    This study reports on the effect of admixed polyethylene oxide-b-polystyrene (PEO113-b-PS70)micelles on corrosion behavior of reinforced mortar. The electrochemical measurement shows that the corrosion performance of the reinforcing steel was not significantly improved. However, surface analysis and

  12. Graphene-Gold Nanoparticles Hybrid-Synthesis, Functionalization, and Application in a Electrochemical and Surface-Enhanced Raman Scattering Biosensor.

    Science.gov (United States)

    Khalil, Ibrahim; Julkapli, Nurhidayatullaili Muhd; Yehye, Wageeh A; Basirun, Wan Jefrey; Bhargava, Suresh K

    2016-05-24

    Graphene is a single-atom-thick two-dimensional carbon nanosheet with outstanding chemical, electrical, material, optical, and physical properties due to its large surface area, high electron mobility, thermal conductivity, and stability. These extraordinary features of graphene make it a key component for different applications in the biosensing and imaging arena. However, the use of graphene alone is correlated with certain limitations, such as irreversible self-agglomerations, less colloidal stability, poor reliability/repeatability, and non-specificity. The addition of gold nanostructures (AuNS) with graphene produces the graphene-AuNS hybrid nanocomposite which minimizes the limitations as well as providing additional synergistic properties, that is, higher effective surface area, catalytic activity, electrical conductivity, water solubility, and biocompatibility. This review focuses on the fundamental features of graphene, the multidimensional synthesis, and multipurpose applications of graphene-Au nanocomposites. The paper highlights the graphene-gold nanoparticle (AuNP) as the platform substrate for the fabrication of electrochemical and surface-enhanced Raman scattering (SERS)-based biosensors in diverse applications as well as SERS-directed bio-imaging, which is considered as an emerging sector for monitoring stem cell differentiation, and detection and treatment of cancer.

  13. Graphene–Gold Nanoparticles Hybrid—Synthesis, Functionalization, and Application in a Electrochemical and Surface-Enhanced Raman Scattering Biosensor

    Science.gov (United States)

    Khalil, Ibrahim; Julkapli, Nurhidayatullaili Muhd; Yehye, Wageeh A.; Basirun, Wan Jefrey; Bhargava, Suresh K.

    2016-01-01

    Graphene is a single-atom-thick two-dimensional carbon nanosheet with outstanding chemical, electrical, material, optical, and physical properties due to its large surface area, high electron mobility, thermal conductivity, and stability. These extraordinary features of graphene make it a key component for different applications in the biosensing and imaging arena. However, the use of graphene alone is correlated with certain limitations, such as irreversible self-agglomerations, less colloidal stability, poor reliability/repeatability, and non-specificity. The addition of gold nanostructures (AuNS) with graphene produces the graphene–AuNS hybrid nanocomposite which minimizes the limitations as well as providing additional synergistic properties, that is, higher effective surface area, catalytic activity, electrical conductivity, water solubility, and biocompatibility. This review focuses on the fundamental features of graphene, the multidimensional synthesis, and multipurpose applications of graphene–Au nanocomposites. The paper highlights the graphene–gold nanoparticle (AuNP) as the platform substrate for the fabrication of electrochemical and surface-enhanced Raman scattering (SERS)-based biosensors in diverse applications as well as SERS-directed bio-imaging, which is considered as an emerging sector for monitoring stem cell differentiation, and detection and treatment of cancer. PMID:28773528

  14. Graphene–Gold Nanoparticles Hybrid—Synthesis, Functionalization, and Application in a Electrochemical and Surface-Enhanced Raman Scattering Biosensor

    Directory of Open Access Journals (Sweden)

    Ibrahim Khalil

    2016-05-01

    Full Text Available Graphene is a single-atom-thick two-dimensional carbon nanosheet with outstanding chemical, electrical, material, optical, and physical properties due to its large surface area, high electron mobility, thermal conductivity, and stability. These extraordinary features of graphene make it a key component for different applications in the biosensing and imaging arena. However, the use of graphene alone is correlated with certain limitations, such as irreversible self-agglomerations, less colloidal stability, poor reliability/repeatability, and non-specificity. The addition of gold nanostructures (AuNS with graphene produces the graphene–AuNS hybrid nanocomposite which minimizes the limitations as well as providing additional synergistic properties, that is, higher effective surface area, catalytic activity, electrical conductivity, water solubility, and biocompatibility. This review focuses on the fundamental features of graphene, the multidimensional synthesis, and multipurpose applications of graphene–Au nanocomposites. The paper highlights the graphene–gold nanoparticle (AuNP as the platform substrate for the fabrication of electrochemical and surface-enhanced Raman scattering (SERS-based biosensors in diverse applications as well as SERS-directed bio-imaging, which is considered as an emerging sector for monitoring stem cell differentiation, and detection and treatment of cancer.

  15. Stainless steel surface biofunctionalization with PMMA-bioglass coatings: compositional, electrochemical corrosion studies and microbiological assay.

    Science.gov (United States)

    Floroian, L; Samoila, C; Badea, M; Munteanu, D; Ristoscu, C; Sima, F; Negut, I; Chifiriuc, M C; Mihailescu, I N

    2015-06-01

    A solution is proposed to surpass the inconvenience caused by the corrosion of stainless steel implants in human body fluids by protection with thin films of bioactive glasses or with composite polymer-bioactive glass nanostructures. Our option was to apply thin film deposition by matrix-assisted pulsed laser evaporation (MAPLE) which, to the difference to other laser or plasma techniques insures the protection of a more delicate material (a polymer in our case) against degradation or irreversible damage. The coatings composition, modification and corrosion resistance were investigated by FTIR and electrochemical techniques, under conditions which simulate their biological interaction with the human body. Mechanical testing demonstrates the adhesion, durability and resistance to fracture of the coatings. The coatings biocompatibility was assessed by in vitro studies and by flow cytometry. Our results support the unrestricted usage of coated stainless steel as a cheap alternative for human implants manufacture. They will be more accessible for lower prices in comparison with the majority present day fabrication of implants using Ti or Ti alloys.

  16. A Facile Surface Reconstruction Mechanism toward Better Electrochemical Performance of Li

    NARCIS (Netherlands)

    Qian, Kun; Tang, Linkai; Wagemaker, M.; He, Yan Bing; Liu, Dongqing; Li, Hai; Shi, Ruiying; Li, Baohua; Kang, Feiyu

    2017-01-01

    Through a facile sodium sulfide (Na2S)-assisted hydrothermal treatment, clean and nondefective surfaces are constructed on micrometer-sized Li4Ti5O12 particles. The remarkable improvement of surface quality shows a higher first cycle Coulombic

  17. Atomic-scale Modelling of Electro-catalytic Surfaces and Dynamic Electrochemical Interfaces

    DEFF Research Database (Denmark)

    Hansen, Martin Hangaard

    This dissertation addresses numerical calculations on the atomic scale to study catalytic surfaces for electrochemistry. The first half of the thesis deals with calculations on the properties of catalytic surfaces, using well known methodology, whereas the second half of the thesis deals with the......This dissertation addresses numerical calculations on the atomic scale to study catalytic surfaces for electrochemistry. The first half of the thesis deals with calculations on the properties of catalytic surfaces, using well known methodology, whereas the second half of the thesis deals...... with the development of new methodology to explicitly include the electrolyte in the atomic scale calculations. Chapter 3 presents calculations on contracted and reconstructed platinum surfaces, which are relevant for development of catalysts for proton exchange membrane fuel cells. Correlation of the results...

  18. The theory of cyclic voltammetry of electrochemically heterogeneous surfaces: comparison of different models for surface geometry and applications to highly ordered pyrolytic graphite.

    Science.gov (United States)

    Ward, Kristopher R; Lawrence, Nathan S; Hartshorne, R Seth; Compton, Richard G

    2012-05-28

    The cyclic voltammetry at electrodes composed of multiple electroactive materials, where zones of one highly active material are distributed over a substrate of a second, less active material, is investigated by simulation. The two materials are assumed to differ in terms of their electrochemical rate constants towards any given redox couple. For a one-electron oxidation or reduction, the effect on voltammetry of the size and relative surface coverages of the zones as well as the rate constant of the slower zone are considered for systems where it is much slower than the rate constant of the faster zones. The occurrence of split peak cyclic voltammetry where two peaks are observed in the forward sweep, is studied in terms of the diffusional effects present in the system. A number of surface geometries are compared: specifically the more active zones are modelled as long, thin bands, as steps in the surface, as discs, and as rings (similar to a partially blocked electrode). Similar voltammetry for the band, step and ring models is seen but the disc geometry shows significant differences. Finally, the simulation technique is applied to the modelling of highly-ordered pyrolytic graphite (HOPG) surface and experimental conditions under which it may be possible to observe split peak voltammetry are predicted.

  19. Improvement of Electrochemical Surface Properties in Steel Substrates Using a Nanostructured CrN/AlN Multilayer Coating

    Science.gov (United States)

    Cabrera, G.; Torres, F.; Caicedo, J. C.; Aperador, W.; Amaya, C.; Prieto, P.

    2012-01-01

    Improvement of corrosion properties on AISI D3 steel surfaces coated with [CrN/AlN] n multilayered system deposited for various periods (Λ) via magnetron sputtering has been studied in this work exhaustively. For practical effects compared were the latter properties with CrN and AlN single layers deposited with the same conditions as the multilayered systems. The coatings were characterized in terms of crystal phase; chemical composition, micro-structural, and electrochemical properties by x-ray diffractometry, energy dispersive x-ray, Fourier transforming infrared spectroscopy, atomic force microscopy, scanning electron microscopy, Tafel polarization curves, and electrochemical impedance spectroscopy. Corrosion evolution was observed via optical microscopy. Results from x-ray diffractometry analysis revealed that the crystal structure of [CrN/AlN] n multilayered coatings has an NaCl-type lattice structure and hexagonal structure (wurtzite-type) for CrN and AlN, respectively, i.e., it was made non-isostructural multilayered. The best behavior was obtained by the multilayered period: Λ = 60 nm (50 bilayers), showing the maximum corrosion resistance (polarization resistance of 1.18 KΩ, and corrosion rate of 1.02 mpy). Those results indicated an improvement of anticorrosive properties, compared to the CrN/AlN multilayer system with 1 bilayer at 98 and 80%, respectively. Furthermore, the corrosion resistance of steel AISI D3 is improved beyond 90%. These improvement effects in multilayered coatings could be attributed to the number of interfaces that act as obstacles for the inward and outward diffusions of ion species, generating an increment in the energy or potential required for translating the corrosive ions across the coating/substrate interface. Moreover, the interface systems affect the means free path on the ions toward the metallic substrate, due to the decreasing of the defects presented in the multilayered coatings.

  20. Preparation of anti-adhesion surfaces on aluminium substrates of rubber plastic moulds using a coupling method of liquid plasma and electrochemical machining

    Directory of Open Access Journals (Sweden)

    Jianbing Meng

    2014-02-01

    Full Text Available Hard anti-adhesion surfaces, with low roughness and wear resistance, on aluminium substrates of rubber plastic moulds were fabricated via a new coupling method of liquid plasma and electrochemical machining. With the aid of liquid plasma thermal polishing and electrochemical anodic dissolution, micro/nano-scale binary structures were prepared as the base of the anti-adhesion surfaces. The anti-adhesion behaviours of the resulting aluminium surfaces were analysed by a surface roughness measuring instrument, a scanning electron microscope (SEM, a Fourier-transform infrared spectrophotometer (FTIR, an X-ray diffractometer (XRD, an optical contact angle meter, a digital Vickers micro-hardness (Hv tester, and electronic universal testing. The results show that, after the liquid plasma and electrochemical machining, micro/nano-scale binary structures composed of micro-scale pits and nano-scale elongated boss structures were present on the sample surfaces. As a result, the anti-adhesion surfaces fabricated by the above coupling method have good anti-adhesion properties, better wear resistance and lower roughness.

  1. Preparation of anti-adhesion surfaces on aluminium substrates of rubber plastic moulds using a coupling method of liquid plasma and electrochemical machining

    Science.gov (United States)

    Meng, Jianbing; Dong, Xiaojuan; Wei, Xiuting; Yin, Zhanmin

    2014-03-01

    Hard anti-adhesion surfaces, with low roughness and wear resistance, on aluminium substrates of rubber plastic moulds were fabricated via a new coupling method of liquid plasma and electrochemical machining. With the aid of liquid plasma thermal polishing and electrochemical anodic dissolution, micro/nano-scale binary structures were prepared as the base of the anti-adhesion surfaces. The anti-adhesion behaviours of the resulting aluminium surfaces were analysed by a surface roughness measuring instrument, a scanning electron microscope (SEM), a Fourier-transform infrared spectrophotometer (FTIR), an X-ray diffractometer (XRD), an optical contact angle meter, a digital Vickers micro-hardness (Hv) tester, and electronic universal testing. The results show that, after the liquid plasma and electrochemical machining, micro/nano-scale binary structures composed of micro-scale pits and nano-scale elongated boss structures were present on the sample surfaces. As a result, the anti-adhesion surfaces fabricated by the above coupling method have good anti-adhesion properties, better wear resistance and lower roughness.

  2. Structure Effects on the Energetics of the Electrochemical Reduction of CO2 by Copper Surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Durand, William

    2011-08-19

    Polycrystalline copper electrocatalysts have been experimentally shown to be capable of reducing CO{sub 2} into CH{sub 4} and C{sub 2}H{sub 4} with relatively high selectivity, and a mechanism has recently been proposed for this reduction on the fcc(211) surface of copper, which was assumed to be the most active facet. In the current work, we use computational methods to explore the effects of the nanostructure of the copper surface and compare the effects of the fcc(111), fcc(100) and fcc(211) facets of copper on the energetics of the electroreduction of CO{sub 2}. The calculations performed in this study generally show that the intermediates in CO{sub 2} reduction are most stabilized by the (211) facet, followed by the (100) facet, with the (111) surface binding the adsorbates most weakly. This leads to the prediction that the (211) facet is the most active surface among the three in producing CH{sub 4} from CO{sub 2}, as well as the by-products H{sub 2} and CO. HCOOH production may be mildly enhanced on the more close-packed surfaces ((111) and (100)) as compared to the (211) facet, due to a change in mechanism from a carboxyl intermediate to a formate intermediate. The results are compared to experimental data on these same surfaces; the predicted trends in voltage requirements are consistent between the experimental and computational data.

  3. Microscopic surface wettability electrochemical characterization of tight sandstone with infrared spectra testing

    Science.gov (United States)

    Song, L.; Ning, Z. F.; Li, N.; Zhang, B.; Ding, G. Y.

    2017-08-01

    The distribution of charge density on the surface of microscopic tight oil is studied by using Stern double electric layer theory, and the mathematical flow model of polar fluid with micro powers in tight oil reservoir is established. The Fourier transform infrared (FTIR) were used to investigate the interaction of rock surface functional groups with fluids. The results show that: (1) When the external fluid of the polar group passes through the dense micro-nano pore, it will form an electric double layer on the surface of the rock, there will be a certain thickness of the liquid membrane, the fluid migration has a certain Of the electrical viscosity effect, will have a certain flow resistance. (2) The Fourier transform infrared spectroscopy of the Chang 7 tight reservoir rock samples exists and distributes different kinds of peaks. The left peak trend determines the presence of hydroxyl groups. The four fronts and types of the right side can be used to obtain that calcium carbonate CO3 2- exists. (3) There are CO3 2- and hydroxyl functional minerals in the Chang 7 tight sandstone samples. It is consistent with the basic mineral analysis measured by X-ray diffraction. When the external fluid affects the rock surface, the surface will occur in the physical van der Waals force and chemical bond interaction, so it will affect the flow of water on the surface.

  4. Surface resistivity/conductivity of different organic-thin films by a combination of optical shearography and electrochemical impedance spectroscopy

    Science.gov (United States)

    Habib, Khaled

    2013-01-01

    Optical shearography and electrochemical impedance spectroscopy (EIS) were used for the first time to measure the surface resistivity/conductivity of different organic-thin films. Different organic coatings i.e., ACE Premium-gray, white, and beige Enamels (spray coatings), on a metallic alloy, i.e., a carbon steel, were investigated at a temperature range between 20-60 °C. The investigation focused on determining the in-plane displacement of the coatings with respect to the applied temperature range by optical shearography. Then, the AC impedance (resistance) of the same coated samples was determined by the technique of EIS in 3.5% NaCl solution at room temperature. In addition, a mathematical model was developed in order to obtain a proportionality constant (surface resistivity = ρ or conductivity = 1/ ρ) between the determined AC impedance and the in-plane displacement. The obtained values of ρ of all investigated coatings, 0:25 × 108-0:27 × 1010 Ωcm was found in the insulator range.

  5. Electrochemical and electrocatalytic studies of toluidine blue immobilized on a silica gel surface coated with niobium oxide

    Directory of Open Access Journals (Sweden)

    Santos Antonio S.

    2002-01-01

    Full Text Available The electrochemical behavior of toluidine blue (TB adsorbed on a silica surface modified with niobium oxide (SN was investigated using a modified carbon paste electrode. The presence of SN gave the electrode high stability, avoiding the leaching out of the mediator from the electrode surface. The formal potential (E0' of the adsorbed TB was --113 mV vs. SCE, indicating a shift of almost 100 mV towards more positive potential values, compared to TB dissolved in aqueous solution or adsorbed on carbon paste. The stability and formal potential remained constant upon changing the solution pH in the range 5 to 8. In these solution pH values the electrocatalytic activity remained almost constant with a sensitivity of 1.2 10-4 A L mol-1 cm-2 and a K Mapp of 4.9 10-5 mol L-1. A linear response range for NADH concentration between 2.0 10-4 and 4.0 10-3 mol L-1 at pH 7.0, with a detection limit of 3.4 10-5 mol L-1 was observed for the sensor. A response time of 2 s and a precision of 1.0 %, expressed as relative standard deviation for 10 replicates, were observed for the sensor developed.

  6. High yield synthesis of some phosphonic acid derivatives as surface ...

    African Journals Online (AJOL)

    Efficient synthesis of novel 6-(2-bromo-2-methyl propanoyloxy)hexyl phosphonic acid, dodecane di-phosphonic acid, 6-(thiophene-3-carbonyloxy)hexyl phosphonic acid, octadecyl phosphonic acid and such other derivatives are reported here. These derivatives have a potential application as tethers to nanoparticle ...

  7. Electrochemical dissolution of surface alloys in acids: Thermodynamic trends from first-principles calculations

    DEFF Research Database (Denmark)

    Greeley, Jeffrey Philip; Nørskov, Jens Kehlet

    2007-01-01

    A simple procedure is introduced to use periodic Density Functional Theory calculations to estimate trends in the thermodynamics of surface alloy dissolution in acidic media. With this approach, the dissolution potentials for solute metal atoms embedded in the surface layer of various host metals...... (referenced to the dissolution potential of the solute in its pure, metallic form) are calculated. Periodic trends in the calculated potentials are found to be related to trends in surface segregation energies of the various solute/host pairs. The effects of water splitting and concomitant hydroxyl adsorption...... on the dissolution potentials are also considered; these effects do not change the potentials for highly oxophilic solutes embedded in less active hosts, but they do decrease the dissolution potential for more inert solutes on oxophilic hosts. Finally, the dissolution of Pt "skin" layers from Pt3X (X = Fe, Co...

  8. Pulse electrochemical machining on Invar alloy: Optical microscopic/SEM and non-contact 3D measurement study of surface analyses

    Energy Technology Data Exchange (ETDEWEB)

    Kim, S.H.; Choi, S.G.; Choi, W.K.; Yang, B.Y. [School of Mechanical Engineering, Inha University, Incheon 402-751 (Korea, Republic of); Lee, E.S., E-mail: leees@dreamwiz.com [Department of Mechanical Engineering, Inha University, Incheon 402-751 (Korea, Republic of)

    2014-09-30

    Highlights: • Invar alloy was electrochemically polished and then subjected to PECM (Pulse Electro Chemical Machining) in a mixture of NaCl, glycerin, and distilled water. • Optical microscopic/SEM and non-contact 3D measurement study of Invar surface analyses. • Analysis result shows that applied voltage and electrode shape are factors that affect the surface conditions. - Abstract: In this study, Invar alloy (Fe 63.5%, Ni 36.5%) was electrochemically polished by PECM (Pulse Electro Chemical Machining) in a mixture of NaCl, glycerin, and distilled water. A series of PECM experiments were carried out with different voltages and different electrode shapes, and then the surfaces of polished Invar alloy were investigated. The polished Invar alloy surfaces were investigated by optical microscope, scanning electron microscope (SEM), and non-contact 3D measurement (white light microscopes) and it was found that different applied voltages produced different surface characteristics on the Invar alloy surface because of the locally concentrated applied voltage on the Invar alloy surface. Moreover, we found that the shapes of electrode also have an effect on the surface characteristics on Invar alloy surface by influencing the applied voltage. These experimental findings provide fundamental knowledge for PECM of Invar alloy by surface analysis.

  9. Functionalized Solid Electrodes for Electrochemical Biosensing of Purine Nucleobases and Their Analogues: A Review

    Directory of Open Access Journals (Sweden)

    Vimal Kumar Sharma

    2015-01-01

    Full Text Available Interest in electrochemical analysis of purine nucleobases and few other important purine derivatives has been growing rapidly. Over the period of the past decade, the design of electrochemical biosensors has been focused on achieving high sensitivity and efficiency. The range of existing electrochemical methods with carbon electrode displays the highest rate in the development of biosensors. Moreover, modification of electrode surfaces based on nanomaterials is frequently used due to their extraordinary conductivity and surface to volume ratio. Different strategies for modifying electrode surfaces facilitate electron transport between the electrode surface and biomolecules, including DNA, oligonucleotides and their components. This review aims to summarize recent developments in the electrochemical analysis of purine derivatives, as well as discuss different applications.

  10. OPTIMIZATION OF PROCESSING PARAMETERS IN ELECTROCHEMICAL MACHINING OF AISI 202 USING RESPONSE SURFACE METHODOLOGY

    Directory of Open Access Journals (Sweden)

    V. SATHIYAMOORTHY

    2015-06-01

    Full Text Available This paper attempts to optimize the predominated machining parameters in Electro Chemical Machining (ECM of AISI 202 Austenitic stainless steel using Response Surface Methodology (RSM. The chosen material has been used in railway rolling stock. The selected influencing parameters are applied voltage, electrolyte discharge rate with three levels and tool feed rate with four levels. Thirty six experiments were conducted through design of experiments and central composite design in RSM was applied to identify the optimum conditions which turn into the best Material Removal Rate (MRR and Surface roughness (SR. The experimental analyses reveal that applied voltage of 16 V, tool feed rate of 0.54 mm/min and electrolyte discharge rate of 10 L/min would be the optimum values in ECM of AISI 202 under the selected conditions. For checking the optimality of the developed equation, MRR of 298.276 mm3/min and surface roughness Ra of 2.05 µm were predicted at applied voltage of 12.5 V, tool feed rate of 0.54 mm/min and electrolyte discharge rate of 11.8 L/min with composite desirability of 98.05%. Confirmatory tests showed that the actual performance at the optimum conditions were 291.351 mm3/min and 2.17 µm. The deviation from the predicted performance is less than 6% which proves the composite desirability of the developed models for MRR and surface roughness.

  11. Electrochemical evaluation of electron transfer kinetics of high and low redox potential laccases on gold electrode surface

    Energy Technology Data Exchange (ETDEWEB)

    Frasconi, Marco [Department of Chemistry and Drug Technologies, Sapienza University of Rome, P.le Aldo Moro, 5 00185 Rome (Italy); Boer, Harry; Koivula, Anu [VTT Technical Research Centre of Finland, P.O. Box 1000, FI-02044 VTT (Finland); Mazzei, Franco, E-mail: franco.mazzei@uniroma1.i [Department of Chemistry and Drug Technologies, Sapienza University of Rome, P.le Aldo Moro, 5 00185 Rome (Italy)

    2010-12-30

    Laccases and other multicopper oxidases are reported to be able to carry out direct electron transfer reactions when immobilized onto electrode surface. This allows detailed research of their electron transfer mechanisms. We have recently characterized the kinetic properties of four laccases in homogenous solution and immobilized onto an electrode surface with respect to a set of different redox mediators. In this paper we report the direct electron transfer of four purified laccases from Trametes hirsuta (ThL), Trametes versicolor (TvL), Melanocarpus albomyces (r-MaL) and Rhus vernicifera (RvL), by trapping the proteins within an electrochemically inert polymer of tributylmethyl phosphonium chloride coating a gold electrode surface. In particular, we have characterized the steps involved in the laccases electron transfer mechanism as well as the factors limiting each step. During the voltammetric experiments, non-turnover Faradic signals with midpoint potential of about 790 and 400 mV were observed for high potential laccases, ThL and TvL, corresponding to redox transformations of the T1 site and the T2/T3 cluster of the enzyme, respectively, whereas low redox potential laccases r-MaL and RvL shown a redox couple with a midpoint potential around 400 mV. The electrocatalytic properties of these laccase modified electrodes for the reduction of oxygen have been evaluated demonstrating significative direct electron transfer kinetics. The biocatalytic activity of laccases was also monitored in the presence of a well known inhibitor, sodium azide. On the basis of the experimental results, a hypothesis about the electronic pathway for intramolecular electron transfer characterizing laccases has been proposed.

  12. Pulse electrochemical machining on Invar alloy: Optical microscopic/SEM and non-contact 3D measurement study of surface analyses

    Science.gov (United States)

    Kim, S. H.; Choi, S. G.; Choi, W. K.; Yang, B. Y.; Lee, E. S.

    2014-09-01

    In this study, Invar alloy (Fe 63.5%, Ni 36.5%) was electrochemically polished by PECM (Pulse Electro Chemical Machining) in a mixture of NaCl, glycerin, and distilled water. A series of PECM experiments were carried out with different voltages and different electrode shapes, and then the surfaces of polished Invar alloy were investigated. The polished Invar alloy surfaces were investigated by optical microscope, scanning electron microscope (SEM), and non-contact 3D measurement (white light microscopes) and it was found that different applied voltages produced different surface characteristics on the Invar alloy surface because of the locally concentrated applied voltage on the Invar alloy surface. Moreover, we found that the shapes of electrode also have an effect on the surface characteristics on Invar alloy surface by influencing the applied voltage. These experimental findings provide fundamental knowledge for PECM of Invar alloy by surface analysis.

  13. ELECTROCHEMICAL PROPERTIES AND ELECTROCHEMICAL ...

    African Journals Online (AJOL)

    b Department of Materials Engineering and Industrial Technologies, University of Trento, 38050. Trento ... KEY WORDS: Conducting polymers, Polypyrrole, Electrochemical impedance spectroscopy, Equivalent- electrical ..... composed of a constant-phase element with exponent values of 0.38-0.67 for PPy/ClO4. -/w and.

  14. Promotional effect of surface hydroxyls on electrochemical reduction of CO2 over SnOx/Sn electrode

    Energy Technology Data Exchange (ETDEWEB)

    Cui, Chaonan; Han, Jinyu; Zhu, Xinli; Liu, Xiao; Wang, Hua; Mei, Donghai; Ge, Qingfeng

    2016-11-01

    Tin oxide (SnOx) formation on tin-based electrode surfaces during CO2 electrochemical reduction can have a significant impact on the activity and selectivity of the reaction. In the present study, density functional theory (DFT) calculations have been performed to understand the role of SnOx in CO2 reduction using a SnO monolayer on the Sn(112) surface as a model for SnOx. Water molecules have been treated explicitly and considered actively participating in the reaction. The results showed that H2O dissociates on the perfect SnO monolayer into two hydroxyl groups symmetrically on the surface. CO2 energetically prefers to react with the hydroxyl, forming a bicarbonate (HCO3(t)*) intermediate, which can then be reduced to either formate (HCOO*) by hydrogenating the carbon atom or carboxyl (COOH*) by protonating the oxygen atom. Both steps involve a simultaneous C-O bond breaking. Further reduction of HCOO* species leads to the formation of formic acid in the acidic solution at pH < 4, while the COOH* will decompose to CO and H2O via protonation. Whereas the oxygen vacancy (VO) in the monolayer maybe formed by the reduction of the monolayer, it can be recovered by H2O dissociation, resulting in two embedded hydroxyl groups. However, the hydroxylated surface with two symmetric hydroxyls is energetically more favorable for CO2 reduction than the hydroxylated VO surface with two embedded hydroxyls. The reduction potential for the former has a limiting-potential of -0.20 V (RHE), lower than that for the latter (-0.74 V (RHE)). Compared to the pure Sn electrode, the formation of SnOx monolayer on the electrode under the operating conditions promotes CO2 reduction more effectively by forming surface hydroxyls, thereby, providing a new channel via COOH* to the CO formation, although formic acid is still the major reduction product. The work was supported in part by National Natural Sciences Foundation of China (Grant #21373148 and #21206117). The High Performance Computing

  15. A new fluorescent and electrochemical Zn2+ ion sensor based on Schiff base derived from benzil and L-tryptophan.

    Science.gov (United States)

    Dutta, Kaku; Deka, Ramesh C; Das, Diganta Kumar

    2014-04-24

    Single molecule acting as both fluorescent and electrochemical sensor for Zn(2+) ion is rare. The product (L) obtained on condensation between benzil and L-tryptophan has been characterized by H NMR, ESI-MS and FT-IR spectroscopy. L in 1:1 (v/v) CH3OH:H2O solution shows fluorescence emission in the range 300 nm to 600 nm with λmax at 350 nm when is excited with 295 nm photon. Zn(2+) ion could induce a 10-fold enhancement in fluorescent intensity of L. Fluorescence and UV/Visible spectral data analysis shows that the binding ratio between Zn(2+) ion and L is 1:1 with log β=4.55. Binding of Zn(2+) ion disrupts the photoinduced electron transfer (PET) process in L and causes the fluorescence intensity enhancement. When cyclic voltammogram is recorded for L in 1:1 (v/v) CH3OH:H2O using glassy carbon (GC) electrode, two quasi reversible redox couples at redox potential values -0.630±0.005 V and -1.007±0.005 V are obtained (Ag-AgCl as reference, scan rate 0.1 V s(-1)). Interaction with Zn(2+) ion makes the first redox couple irreversible while the second couple undergoes a 0.089 V positive shift in redox potential. Metal ions - Cd(2+), Cu(2+), Co(2+), Hg(2+), Ag(+), Ni(2+), Fe(2+), Mn(2+), Mg(2+), Ca(2+)and Pb(2+), individually or all together, has no effect on the fluorescent as well as electrochemical property of L. DFT calculations showed that Zn(2+) ion binds to L to form a stable complex. The detection limit for both fluorescence as well as electrochemical detection was 10(-6) M. Copyright © 2013 Elsevier B.V. All rights reserved.

  16. Density functional theory study of carbon dioxide electrochemical reduction on the Fe(100) surface.

    Science.gov (United States)

    Bernstein, Nicole J; Akhade, Sneha A; Janik, Michael J

    2014-07-21

    Carbon dioxide electroreduction offers the possibility of producing hydrocarbon fuels using energy from renewable sources. Herein, we use density functional theory to analyze the feasibility of CO2 electroreduction on a Fe(100) surface. Experimentally, iron is nonselective for hydrocarbon formation. A simplistic analysis of low-coverage reaction intermediate energies for the paths to produce CH4 and CH3OH from CO2 suggests Fe(100) could be more active than Cu(111), currently the only metallic catalyst to show selectivity towards hydrocarbon formation. We consider a series of impediments to CO2 electroreduction on Fe(100) including O*/OH* (* denotes surface bound species) blockage of active surface sites; competitive adsorption effects of H*, CO* and C*; and iron carbide formation. Our results indicate that under CO2 electroreduction conditions, Fe(100) is predicted to be covered in C* or CO* species, blocking any C-H bond formation. Further, bulk Fe is predicted to be unstable relative to FeCx formation at potentials relevant to CO2 electroreduction conditions.

  17. Electrochemical Surface Treatment of a β-titanium Alloy to Realize an Antibacterial Property and Bioactivity

    Directory of Open Access Journals (Sweden)

    Yusuke Tsutsumi

    2016-03-01

    Full Text Available In this study, micro-arc oxidation (MAO was performed on a β-type titanium alloy, namely, Ti-29Nb-13Ta-4.6Zr alloy (TNTZ, to improve not only its antibacterial property but also bioactivity in body fluids. The surface oxide layer formed on TNTZ by MAO treatment in a mixture of calcium glycerophosphate, calcium acetate, and silver nitrate was characterized using surface analyses. The resulting porous oxide layer was mainly composed of titanium oxide, and it also contained calcium, phosphorus, and a small amount of silver, all of which were incorporated from the electrolyte during the treatment. The MAO-treated TNTZ showed a strong inhibition effect on anaerobic Gram-negative bacteria when the electrolyte contained more than 0.5 mM silver ions. The formation of calcium phosphate on the surface of the specimens after immersion in Hanks’ solution was evaluated to determine the bioactivity of TNTZ with sufficient antibacterial property. As a result, thick calcium phosphate layers formed on the TNTZ specimen that underwent MAO treatment, whereas no precipitate was observed on TNTZ without treatment. Thus, the MAO treatment of titanium-based alloys is confirmed to be effective in realizing both antibacterial and bioactive properties.

  18. Electrochemical surface functionalization of carbon fibers for chemical affinity improvement with epoxy resins

    Science.gov (United States)

    Kainourgios, Panayiotis; Kartsonakis, Ioannis A.; Dragatogiannis, Dimitrios A.; Koumoulos, Elias P.; Goulis, Panagiotis; Charitidis, Costas A.

    2017-09-01

    The purpose of this study is to increase the wetting properties of carbon fibers in order to improve the adhesion force between the fiber and the polymer matrix. Commercial carbon fibers were surface functionalized through cyclic voltammetry together with potentiostatic conditions in aqueous electrolyte solutions of H2SO4, in the presence of acrylic acid, methacrylic acid, acrylonitrile and N-vinylpyrrolidone monomers. The anodic and cathodic peaks were correlated with oxide formation and their partial reduction, respectively. The produced surface modified carbon fibers were wetted with epoxy resin so that to produce dumbbell type composites for tensile strength testing. The nature of oxygen containing groups on the fibers surface was determined by Fourier-transform infrared and Raman spectroscopy. Moreover, the wetting properties of the treated carbon fibers were evaluated via contact angle measurements whereas the morphology of the coated fibers was investigated via scanning electron microscopy. Finally, the mechanical performance of the composites was evaluated by means of tensile testing and strength measurements.

  19. Why Do We Need the Derivative for the Surface Area?

    Science.gov (United States)

    Hristova, Yulia; Zeytuncu, Yunus E.

    2016-01-01

    Surface area and volume computations are the most common applications of integration in calculus books. When computing the surface area of a solid of revolution, students are usually told to use the frustum method instead of the disc method; however, a rigorous explanation is rarely provided. In this note, we provide one by using geometric…

  20. Using SMOS brightness temperature and derived surface-soil moisture to characterize surface conditions and validate land surface models.

    Science.gov (United States)

    Polcher, Jan; Barella-Ortiz, Anaïs; Piles, Maria; Gelati, Emiliano; de Rosnay, Patricia

    2017-04-01

    The SMOS satellite, operated by ESA, observes the surface in the L-band. On continental surface these observations are sensitive to moisture and in particular surface-soil moisture (SSM). In this presentation we will explore how the observations of this satellite can be exploited over the Iberian Peninsula by comparing its results with two land surface models : ORCHIDEE and HTESSEL. Measured and modelled brightness temperatures show a good agreement in their temporal evolution, but their spatial structures are not consistent. An empirical orthogonal function analysis of the brightness temperature's error identifies a dominant structure over the south-west of the Iberian Peninsula which evolves during the year and is maximum in autumn and winter. Hypotheses concerning forcing-induced biases and assumptions made in the radiative transfer model are analysed to explain this inconsistency, but no candidate is found to be responsible for the weak spatial correlations. The analysis of spatial inconsistencies between modelled and measured TBs is important, as these can affect the estimation of geophysical variables and TB assimilation in operational models, as well as result in misleading validation studies. When comparing the surface-soil moisture of the models with the product derived operationally by ESA from SMOS observations similar results are found. The spatial correlation over the IP between SMOS and ORCHIDEE SSM estimates is poor (ρ 0.3). A single value decomposition (SVD) analysis of rainfall and SSM shows that the co-varying patterns of these variables are in reasonable agreement between both products. Moreover the first three SVD soil moisture patterns explain over 80% of the SSM variance simulated by the model while the explained fraction is only 52% of the remotely sensed values. These results suggest that the rainfall-driven soil moisture variability may not account for the poor spatial correlation between SMOS and ORCHIDEE products. Other reasons have to

  1. Rapid extraction and quantitative detection of the herbicide diuron in surface water by a hapten-functionalized carbon nanotubes based electrochemical analyzer.

    Science.gov (United States)

    Sharma, Priyanka; Bhalla, Vijayender; Tuteja, Satish; Kukkar, Manil; Suri, C Raman

    2012-05-21

    A solid phase extraction micro-cartridge containing a non-polar polystyrene absorbent matrix was coupled with an electrochemical immunoassay analyzer (EIA) and used for the ultra-sensitive detection of the phenyl urea herbicide diuron in real samples. The EIA was fabricated by using carboxylated carbon nanotubes (CNTs) functionalized with a hapten molecule (an amine functionalized diuron derivative). Screen printed electrodes (SPE) were modified with these haptenized CNTs and specific in-house generated anti diuron antibodies were used for bio-interface development. The immunodetection was realized in a competitive electrochemical immunoassay format using alkaline phosphatase labeled secondary anti-IgG antibody. The addition of 1-naphthyl phosphate substrate resulted in the production of an electrochemically active product, 1-naphthol, which was monitored by using differential pulse voltammetry (DPV). The assay exhibited excellent sensitivity and specificity having a dynamic response range of 0.01 pg mL(-1) to 10 μg mL(-1) for diuron with a limit of detection of around 0.1 pg mL(-1) (n = 3) in standard water samples. The micro-cartridge coupled hapten-CNTs modified SPE provided an effective and efficient electrochemical immunoassay for the real-time monitoring of pesticides samples with a very high degree of sensitivity.

  2. Surface structure and electrochemical properties of platinum films grown on SrTiO3(100) substrates

    Science.gov (United States)

    Kasai, Masahiro; Dohi, Hideyuki

    2017-12-01

    We fabricated Pt films on SrTiO3 (STO)(100) using a DC-magnetron sputtering method to investigate the preferred orientation, surface structure, and electrochemical property. A film grown at 400 °C showed the two-dimensional polycrystalline features of Pt(111). Reflection high-energy electron diffraction (RHEED) showed diffraction patterns independent of the in-plane incident angle of the film. Films grown at 600 and 700 °C exhibited a preferred orientation of Pt(100) and (110). The films exhibited the morphology of faceted islands with roughness of several tens of nm, which consisted of two kinds of domains, namely a domain with preferred orientation of (100) and one with (110). The (100) and (110) domains had 45-degree twin boundaries, which were observed as V-shaped streaks by RHEED. The (100) domain was aligned in orientation of [011]Pt//[010]STO, which suggests that the binding strength of the (110) plane at the interface was larger than that of the (100). With a further increase in the growth temperature up to 750 °C, the film primarily showed a preferred orientation of (100) with an in-plane orientation of [010]Pt//[010]STO. The film also showed an island structure; however, atomic force microscopy revealed that the top was atomically flat.

  3. In situ chemical reductive growth of platinum nanoparticles on indium tin oxide surfaces and their electrochemical applications.

    Science.gov (United States)

    Chang, Gang; Oyama, Munetaka; Hirao, Kazuyuki

    2006-02-02

    Platinum nanoparticles directly attached to indium tin oxide (PtNP/ITO) were successfully fabricated by using an in situ chemical reductive growth method. In this method, PtNPs could be grown on the ITO surface via the one-step immersion into the growth solution containing PtCl4(2-) and ascorbic acid. The attached and grown PtNPs were spherical having an agglomerated nanostructure composed of small nanoclusters. From the morphological changes depending on the growth time, which were observed with an FE-SEM, PtNPs were found to be grown via the progressive nucleation mechanism. As the characteristics of the PtNP/ITO were those of a working electrode, it was found that the charge transfer resisivity was significantly lowered due to the grown PtNPs. Hence, for a typical redox system of [Fe(CN)6]3-/[Fe(CN)6]4-, the PtNP/ITO electrode exhibited the electrochemical responses similar to those of the bulk Pt electrode. Furthermore, it was clarified that the PtNP/ITO electrode had significant electrocatalytic properties for the oxygen reduction and methanol oxidation. The present PtNPs that had the agglomerated nanostructure may be promising for a new type of electrode material.

  4. Potential amoebicidal activity of hydrazone derivatives: synthesis, characterization, electrochemical behavior, theoretical study and evaluation of the biological activity.

    Science.gov (United States)

    Toledano-Magaña, Yanis; García-Ramos, Juan Carlos; Navarro-Olivarria, Marisol; Flores-Alamo, Marcos; Manzanera-Estrada, Mayra; Ortiz-Frade, Luis; Galindo-Murillo, Rodrigo; Ruiz-Azuara, Lena; Meléndrez-Luevano, Ruth Ma; Cabrera-Vivas, Blanca M

    2015-05-29

    Four new hydrazones were synthesized by the condensation of the selected hydrazine and the appropriate nitrobenzaldehyde. A complete characterization was done employing 1H- and 13C-NMR, electrochemical techniques and theoretical studies. After the characterization and electrochemical analysis of each compound, amoebicidal activity was tested in vitro against the HM1:IMSS strain of Entamoeba histolytica. The results showed the influence of the nitrobenzene group and the hydrazone linkage on the amoebicidal activity. meta-Nitro substituted compound 2 presents a promising amoebicidal activity with an IC50 = 0.84 μM, which represents a 7-fold increase in cell growth inhibition potency with respect to metronidazole (IC50 = 6.3 μM). Compounds 1, 3, and 4 show decreased amoebicidal activity, with IC50 values of 7, 75 and 23 µM, respectively, as a function of the nitro group position on the aromatic ring. The observed differences in the biological activity could be explained not only by the redox potential of the molecules, but also by their capacity to participate in the formation of intra- and intermolecular hydrogen bonds. Redox potentials as well as the amoebicidal activity can be described with parameters obtained from the DFT analysis.

  5. Coffee Waste-Derived Hierarchical Porous Carbon as a Highly Active and Durable Electrocatalyst for Electrochemical Energy Applications.

    Science.gov (United States)

    Chung, Dong Young; Son, Yoon Jun; Yoo, Ji Mun; Kang, Jin Soo; Ahn, Chi-Yeong; Park, Subin; Sung, Yung-Eun

    2017-11-14

    Nitrogen-doped porous carbon materials have been highlighted as promising alternatives to high-cost platinum in various electrochemical energy applications. However, protocols to generate effective pore structure are still challenging, which hampers mass production and utilization of carbon materials. Here, we suggest a facile and effective method for hierarchical porous carbon by a single-step carbonization of coffee waste (CW) with ZnCl2. The CW, which is one of the most earth-abundant organic waste, can be successfully converted to nitrogen-doped porous carbon. It shows outstanding oxygen reduction activity and durability comparable to the state-of-the-art platinum, and the half-wave potential is also comparable to the best metal-free electrocatalysts in alkaline media. Finally, we apply it to counter electrode of dye-sensitized solar cell, whose photovoltaic efficiency surpasses the one made with conventional platinum electrode. We demonstrate the feasibility of our strategies for highly efficient, cheap, and environment-friendly electrocatalyst to replace platinum in various electrochemical energy applications.

  6. Novel polymer Li-ion binder carboxymethyl cellulose derivative enhanced electrochemical performance for Li-ion batteries.

    Science.gov (United States)

    Qiu, Lei; Shao, Ziqiang; Wang, Daxiong; Wang, Feijun; Wang, Wenjun; Wang, Jianquan

    2014-11-04

    Novel water-based binder lithium carboxymethyl cellulose (CMC-Li) is synthesized by cotton as raw material. The mechanism of the CMC-Li as a binder is reported. Electrochemical properties of batteries' cathodes based on commercially available lithium iron phosphate (LiFePO4, LFP) and water-soluble binder are investigated. Sodium carboxymethyl cellulose (CMC-Na, CMC) and CMC-Li are used as the binder. After 200 cycles, compared with conventional poly(vinylidene fluoride) (PVDF) binder, the CMC-Li binder significantly improves cycling performance of the LFP cathode 96.7% of initial reversible capacity achieved at 175 mA h g(-1). Constant current charge-discharge test results demonstrate that the LFP electrode using CMC-Li as the binder has the highest rate capability, followed closely by those using CMC and PVDF binders, respectively. Electrochemical impedance spectroscopy test results show that the electrode using CMC-Li as the binder has lower charge transfer resistance than the electrodes using CMC and PVDF as the binders. Copyright © 2014 Elsevier Ltd. All rights reserved.

  7. Synthesis and Electrochemical Characterization of M2Mn3O8 (M=Ca,Cu) Compounds and Derivatives

    Energy Technology Data Exchange (ETDEWEB)

    Park, Yong Joon; Doeff, Marca M.

    2005-08-25

    M{sub 2}Mn{sub 3}O{sub 8} (M=Ca{sup 2+}, Cu{sup 2+}) compounds were synthesized and characterized in lithium cells. The M{sup 2+} cations, which reside in the van der Waal's gaps between adjacent sheets of Mn{sub 3}O{sub 8}{sup 4-}, may be replaced chemically (by ion-exchange) or electrochemically with Li. More than 7 Li{sup +}/Cu{sub 2}Mn{sub 3}O{sub 8} may be inserted electrochemically, with concomitant reduction of Cu{sup 2+} to Cu metal, but less Li can be inserted into Ca{sub 2}Mn{sub 3}O{sub 8}. In the case of Cu{sup 2+}, this process is partially reversible when the cell is charged above 3.5 V vs. Li, but intercalation of Cu{sup +} rather than Cu{sup 2+} and Li{sup +}/Cu{sup +} exchange occurs during the subsequent discharge. If the cell potential is kept below 3.4 V, the Li in excess of 4Li{sup +}/Cu{sub 2}Mn{sub 3}O{sub 8} can be cycled reversibly. The unusual mobility of +2 cations in a layered structure has important implications both for the design of cathodes for Li batteries and for new systems that could be based on M{sup 2+} intercalation compounds.

  8. Fabrication of a Horizontal and a Vertical Large Surface Area Nanogap Electrochemical Sensor

    Directory of Open Access Journals (Sweden)

    Jules L. Hammond

    2016-12-01

    Full Text Available Nanogap sensors have a wide range of applications as they can provide accurate direct detection of biomolecules through impedimetric or amperometric signals. Signal response from nanogap sensors is dependent on both the electrode spacing and surface area. However, creating large surface area nanogap sensors presents several challenges during fabrication. We show two different approaches to achieve both horizontal and vertical coplanar nanogap geometries. In the first method we use electron-beam lithography (EBL to pattern an 11 mm long serpentine nanogap (215 nm between two electrodes. For the second method we use inductively-coupled plasma (ICP reactive ion etching (RIE to create a channel in a silicon substrate, optically pattern a buried 1.0 mm × 1.5 mm electrode before anodically bonding a second identical electrode, patterned on glass, directly above. The devices have a wide range of applicability in different sensing techniques with the large area nanogaps presenting advantages over other devices of the same family. As a case study we explore the detection of peptide nucleic acid (PNA−DNA binding events using dielectric spectroscopy with the horizontal coplanar device.

  9. Enhancing Electrochemical Water-Splitting Kinetics by Polarization-Driven Formation of Near-Surface Iron(0): An In Situ XPS Study on Perovskite-Type Electrodes**

    Science.gov (United States)

    Opitz, Alexander K; Nenning, Andreas; Rameshan, Christoph; Rameshan, Raffael; Blume, Raoul; Hävecker, Michael; Knop-Gericke, Axel; Rupprechter, Günther; Fleig, Jürgen; Klötzer, Bernhard

    2015-01-01

    In the search for optimized cathode materials for high-temperature electrolysis, mixed conducting oxides are highly promising candidates. This study deals with fundamentally novel insights into the relation between surface chemistry and electrocatalytic activity of lanthanum ferrite based electrolysis cathodes. For this means, near-ambient-pressure X-ray photoelectron spectroscopy (NAP-XPS) and impedance spectroscopy experiments were performed simultaneously on electrochemically polarized La0.6Sr0.4FeO3−δ (LSF) thin film electrodes. Under cathodic polarization the formation of Fe0 on the LSF surface could be observed, which was accompanied by a strong improvement of the electrochemical water splitting activity of the electrodes. This correlation suggests a fundamentally different water splitting mechanism in presence of the metallic iron species and may open novel paths in the search for electrodes with increased water splitting activity. PMID:25557533

  10. second vertical derivatives and trend surface analysis of the ...

    African Journals Online (AJOL)

    DJFLEX

    900. Gunn, P.J., 1997. Quantitative methods for interpreting aeromagnetic data: a subjective review; AGSO. Journal of Australian Geology and Geophysics,. 17,(2): pp.105 -113. Gupta, V.H. and Ramani, S.D., 1982. Optimum second vertical derivative application in geologic mapping and mineral exploration; Geophysics,.

  11. Electrochemical characterization of surface-modified negative electrodes consisting of hydrogen storage alloys

    Energy Technology Data Exchange (ETDEWEB)

    Matsuoka, Masao (Dept. of Applied Chemistry, Univ. of Osaka (Japan)); Asai, Katsuhiko (Dept. of Applied Chemistry, Univ. of Osaka (Japan)); Asai, Kazuaki (Dept. of Applied Chemistry, Univ. of Osaka (Japan)); Fukumoto, Yukio (Dept. of Applied Chemistry, Univ. of Osaka (Japan)); Iwakura, Chiaki (Dept. of Applied Chemistry, Univ. of Osaka (Japan))

    1993-02-23

    Negative electrodes consisting of MmNi[sub 3.6]Mn[sub 0.4]Al[sub 0.3]Co[sub 0.7] alloy powder filled in a porous nickel substrate were modified by using different electroless plating baths or alkaline solutions containing hypophosphite as a reducing agent. The deposited metals function as a microcurrent collector and then increase the discharge capacity of the negative electrodes. In constrast, modification with a reducing agent gives rise to high electrocatalytic activity of the negative electrodes which leads to a remarkable reduction in overvoltage in charging and discharging even at the first cycle. It was found that such simple surface modifications improved the performance of negative electrodes under appropriate conditions with respect to the amount of electroless deposit or the concentration of reducing agent. (orig.)

  12. Surface planarization effect of siloxane derivatives in organic semiconductor layers

    Energy Technology Data Exchange (ETDEWEB)

    Sakanoue, Kei [Center for Organic Photonics and Electronics Research, Kyushu University, Nishi-ku, Fukuoka 819-0395 (Japan); Harada, Hironobu; Ando, Kento [Department of Chemical Engineering, Graduate School of Engineering, Kyushu University, Nishi-ku, Fukuoka 819-0395 (Japan); Yahiro, Masayuki [Institute of Systems, Information Technologies and Nanotechnologies, 2-1-22, Sawara-ku, Fukuoka 814-0001 (Japan); Fukai, Jun, E-mail: jfukai@chem-eng.kyushu-u.ac.jp [Department of Chemical Engineering, Graduate School of Engineering, Kyushu University, Nishi-ku, Fukuoka 819-0395 (Japan)

    2015-12-31

    The ability of siloxane surface control additives (SCAs) to planarize organic semiconductor films with a thickness of tens of nanometers printed on indium tin oxide (ITO) surfaces with stripe-patterned bank structures using a liquid-phase method is demonstrated. Three types of SCAs with different molecular structures are examined in organic solutions of toluene, anisole and tetralin containing N,N′-bis(3-methylphenyl)-N,N′-bis(phenyl)-benzidine as a solute and typical organic semiconductor. While there is an optimum SCA and concentration for each solution, one type of SCA is comprehensively effective for all solutions. This SCA increased contact angle, which is contrary to the typical behavior of SCAs. Scanning electron microscope images of the thin films near the banks reveal that this SCA did not change the contact area between the film and substrate surface, which is related to the effectiveness of the SCA. SCAs did not affect the current–voltage characteristics of green organic light-emitting diodes, but did increase external quantum efficiencies, suggesting that SCAs can be used to improve the quality of solution-deposited films for use in optical devices. - Highlights: • Surface control additives planarize organic semiconductor films coated on surfaces. • The most effective additive increases the contact angle of solutions during drying. • The effect of additives is deduced from solutal Marangoni forces. • Additives have little effect on organic light-emitting diode performance.

  13. Surface enhanced Raman scattering in a nonaqueous electrochemical cell: Pyridine, benzoic acid, and nitrobenzene in methanol

    Science.gov (United States)

    Shin, Gyu-Seung; Kim, Jong-Jean

    1985-07-01

    We have studied SERS on the following systems for comparison between aqueous and nonaqueous media: (1a) {0.05M pyridine}/{2×10 -3fM {KCI}/{methanol}}, (1b) {0.05M pyridine}/{2×10 -3M {KCl}/{water}}, (2a) {0.05M henzoic acid}/{2×10 -3M {KCI}/{methanol}}, (2b) {5×10 -3M benzoic acid }/{2×10 -3M {KCl}/{water}}, and (3) {0.05M nitrobenzene}/{2×10 -3M {KCI}/{methanol}}. As already reported, the surface adsorbed SERS species seem to be the same, irrespective of whether the solvent is water or methanol. However, considerable differences are found in small details between the nonaqueous and the aqueous SERS spectra, the significance of which is discussed in terms of both electrochemistry and SERS. For nitrobenzene, the observed SERS spectra did not show the Raman lines of the original nitrobenzene but some reduction products of nitrobenzene, probably aniline and phenylhydroxylamine.

  14. Tunable Surface Structuration of Silicon by Metal Assisted Chemical Etching with Pt Nanoparticles under Electrochemical Bias.

    Science.gov (United States)

    Torralba, Encarnación; Le Gall, Sylvain; Lachaume, Raphaël; Magnin, Vincent; Harari, Joseph; Halbwax, Mathieu; Vilcot, Jean-Pierre; Cachet-Vivier, Christine; Bastide, Stéphane

    2016-11-16

    An in-depth study of metal assisted chemical etching (MACE) of p-type c-Si in HF/H2O2 aqueous solutions using Pt nanoparticles as catalysts is presented. Combination of cyclic voltammetry, open circuit measurements, chronoamperometry, impedance spectroscopy, and 2D band bending modeling of the metal/semiconductor/electrolyte interfaces at the nanoscale and under different etching conditions allows gaining physical insights into this system. Additionally, in an attempt to mimic the etching conditions, the modeling has been performed with a positively biased nanoparticle buried in the Si substrate. Following these findings, the application of an external polarization during etching is introduced as a novel efficient approach for achieving straightforward control of the pore morphology by acting upon the band bending at the Si/electrolyte junction. In this way, nanostructures ranging from straight mesopores to cone-shaped macropores are obtained as the Si sample is biased from negative to positive potentials. Remarkably, macroscopic cone-shaped pores in the 1-5 μm size range with a high aspect ratio (L/W ∼ 1.6) are obtained by this method. This morphology leads to a reduction of the surface reflectance below 5% over the entire VIS-NIR domain, which outperforms macrostructures made by state of the art texturization techniques for Si solar cells.

  15. The construction of drape surfaces with constrained first derivatives

    Directory of Open Access Journals (Sweden)

    R.J. Fossati

    2014-01-01

    Full Text Available The need to construct optimal drape surfaces arises in airborne geophysical surveys where it is necessary to fly a safe distance above the ground and within the performance of the aircraft used, but as close as possible to the surface. The problem is formulated as an LP with constraints at every point of a grid covering the area concerned, yielding a huge problem. The lifting algorithm is suggested. This is a surprisingly simple algorithm which starts with the drape surface at ground level and lifts it one point at a time. Only points which are too low relative to one or more of their neighbours are considered and they are lifted just enough to bring them into kilter with their neighbours. It is shown that the lifting algorithm is both exact and has great speed advantages. Some numerical results confirming exactness and speed are presented. An enhanced method with better complexity is proposed and tested numerically.

  16. Reproducibility of crop surface maps extracted from Unmanned Aerial Vehicle (UAV) derived digital surface maps

    KAUST Repository

    Parkes, Stephen

    2016-10-25

    Crop height measured from UAVs fitted with commercially available RGB cameras provide an affordable alternative to retrieve field scale high resolution estimates. The study presents an assessment of between flight reproducibility of Crop Surface Maps (CSM) extracted from Digital Surface Maps (DSM) generated by Structure from Motion (SfM) algorithms. Flights were conducted over a centre pivot irrigation system covered with an alfalfa crop. An important step in calculating the absolute crop height from the UAV derived DSM is determining the height of the underlying terrain. Here we use automatic thresholding techniques applied to RGB vegetation index maps to classify vegetated and soil pixels. From interpolation of classified soil pixels, a terrain map is calculated and subtracted from the DSM. The influence of three different thresholding techniques on CSMs are investigated. Median Alfalfa crop heights determined with the different thresholding methods varied from 18cm for K means thresholding to 13cm for Otsu thresholding methods. Otsu thresholding also gave the smallest range of crop heights and K means thresholding the largest. Reproducibility of median crop heights between flight surveys was 4-6cm for all thresholding techniques. For the flight conducted later in the afternoon shadowing caused soil pixels to be classified as vegetation in key locations around the domain, leading to lower crop height estimates. The range of crop heights was similar for both flights using K means thresholding (35-36cm), local minimum thresholding depended on whether raw or normalised RGB intensities were used to calculate vegetation indices (30-35cm), while Otsu thresholding had a smaller range of heights and varied most between flights (26-30cm). This study showed that crop heights from multiple survey flights are comparable, however, they were dependent on the thresholding method applied to classify soil pixels and the time of day the flight was conducted.

  17. Synergetic signal amplification based on electrochemical reduced graphene oxide-ferrocene derivative hybrid and gold nanoparticles as an ultra-sensitive detection platform for bisphenol A

    Energy Technology Data Exchange (ETDEWEB)

    Huang, Na; Liu, Meiling, E-mail: liumeilingww@126.com; Li, Haitao; Zhang, Youyu; Yao, Shouzhuo

    2015-01-01

    Highlights: • A novel (4-ferrocenylethyne) phenylamine was firstly covalently grafted onto GO. • The rGO-Fc-NH{sub 2}/AuNPs composite has good conductivity and compatibility. • The nanocomposite effectively prevent the electron mediator leaking from electrode. • A synergetic amplification platform to ultra-sensitive detect BPA was established. - Abstract: In this paper, a novel electro-active graphene oxide (GO) nanocomposite was firstly prepared by covalently grafted (4-ferrocenylethyne) phenylamine (Fc-NH{sub 2}) onto the surface of GO. The synthesized hybridized nanocomposite of GO-Fc-NH{sub 2} coupled with HAuCl{sub 4} simultaneously electrodeposited on the glassy carbon electrodes (GCE) to obtain rGO-Fc-NH{sub 2}/AuNPs/GCE. The covalently grafted material of the rGO-Fc-NH{sub 2}/AuNPs film can effectively prevent the electron mediator leaking from the electrode surface, which can hold the advantage of both the nanomaterials and electron mediator. By employing the catalysis effect of the nanomaterial and electron mediator coupling with large active surface area and high accumulation capacity of rGO-Fc-NH{sub 2}/AuNPs, a synergetic signal amplification platform for ultra-sensitive detection of bisphenol A (BPA) was successfully established. With this novel sensor, the oxidation peak currents of BPA were linearly dependent on the BPA concentrations in the range of 0.005–10 μM with the detection limit of 2 nM. Modification of electron mediators on nanomaterials can greatly enhance the electrochemical performance of the sensors and will provide a new concept for fabricating newly electro-active nanomaterials-based electrochemical biosensors.

  18. Electrochemical micromachining: An introduction

    Directory of Open Access Journals (Sweden)

    Rebecca J Leese

    2016-01-01

    Full Text Available Electrochemical machining is a relatively new technique, only being introduced as a commercial technique within the last 70 years. A lot of research was conducted in the 1960s and 1970s, but research on electrical discharge machining around the same time slowed electrochemical machining research. The main influence for the development of electrochemical machining came from the aerospace industry where very hard alloys were required to be machined without leaving a defective layer in order to produce a component which would behave reliably. Electrochemical machining was primarily used for the production of gas turbine blades or to machine materials into complex shapes that would be difficult to machine using conventional machining methods. Tool wear is high and the metal removal rate is slow when machining hard materials with conventional machining methods such as milling. This increases the cost of the machining process overall and this method creates a defective layer on the machined surface. Whereas with electrochemical machining there is virtually no tool wear even when machining hard materials and it does not leave a defective layer on the machined surface. This article reviews the application of electrochemical machining with regards to micro manufacturing and the present state of the art micro electrochemical machining considering different machined materials, electrolytes and conditions used.

  19. Northern South China Sea Surface Circulation and its Variability Derived by Combining Satellite Altimetry and Surface Drifter Data

    Directory of Open Access Journals (Sweden)

    N. Peter Benny

    2015-01-01

    Full Text Available The present study analyses the mean and seasonal mesoscale surface circulation of the Northern South China Sea (NSCS and determines the influence of El Niño/SouthernNiño/Southern Oscillation (ENSO. High resolution Eulerian velocity field is derived by combining the available satellite tracked surface drifter data with satellite altimetry during 1993 - 2012. The wind driven current is computed employing the weekly ocean surface mean wind fields derived from the scatterometers on board ERS 1/2, QuikSCAT and ASCAT. The derived mean velocity field exhibits strong boundary currents and broad zonal flow across NSCS. The anomalous field is quite strong in the southern part and the Seasonal circulation clearly depicts the monsoonal forcing. Eddy Kinetic Energy (EKE distribution and its spatial and temporal structures are determined employing Empirical Orthogonal Function (EOF analysis. The ENSO influence on NSCS surface circulation has been analyzed using monthly absolute geostrophic velocity fields during 1996 - 1999.

  20. Do measures matter? Comparing surface-density-derived and census-tract-derived measures of racial residential segregation.

    Science.gov (United States)

    Kramer, Michael R; Cooper, Hannah L; Drews-Botsch, Carolyn D; Waller, Lance A; Hogue, Carol R

    2010-06-12

    Racial residential segregation is hypothesized to affect population health by systematically patterning health-relevant exposures and opportunities according to individuals' race or income. Growing interest into the association between residential segregation and health disparities demands more rigorous appraisal of commonly used measures of segregation. Most current studies rely on census tracts as approximations of the local residential environment when calculating segregation indices of either neighborhoods or metropolitan areas. Because census tracts are arbitrary in size and shape, reliance on this geographic scale limits understanding of place-health associations. More flexible, explicitly spatial derivations of traditional segregation indices have been proposed but have not been compared with tract-derived measures in the context of health disparities studies common to social epidemiology, health demography, or medical geography. We compared segregation measured with tract-derived as well as GIS surface-density-derived indices. Measures were compared by region and population size, and segregation measures were linked to birth record to estimate the difference in association between segregation and very preterm birth. Separate analyses focus on metropolitan segregation and on neighborhood segregation. Across 231 metropolitan areas, tract-derived and surface-density-derived segregation measures are highly correlated. However overall correlation obscures important differences by region and metropolitan size. In general the discrepancy between measure types is greatest for small metropolitan areas, declining with increasing population size. Discrepancies in measures are greatest in the South, and smallest in Western metropolitan areas. Choice of segregation index changed the magnitude of the measured association between segregation and very preterm birth. For example among black women, the risk ratio for very preterm birth in metropolitan areas changed from 2

  1. Structure effect of some amine derivatives on corrosion inhibition efficiency for carbon steel in acidic media using electrochemical and Quantum Theory Methods

    Directory of Open Access Journals (Sweden)

    Ahmed M. Al-Sabagh

    2013-06-01

    Full Text Available The structure effect on corrosion inhibition of two amines and their derivatives is the main object of this article. The first amine was 1,8-diaminooctane and its ethoxylated (50 e.o. 1,8-diaminooctane and propoxylated (50 p.o. 1,8-diaminooctane. The second amine is the tetraethylenepentamine and its ethoxylated (50 e.o. and propoxylated (50 p.o. derivatives. The investigations were carried out by open circuit potential, potentiodynamic polarization, electrochemical impedance, quantum calculations and SEM measurements. The data obtained for the first amine showed the minimum inhibition efficiency (65.5%, meanwhile the maximum inhibition efficiency was 78.9% for its propoxylated derivative. On the other hand the maximium inhibition efficiency was 91% for the second propoxylated amine. The electronic properties; HOMO and LUMO energy levels, energy gap, dipole moment, polarizability, log P, total energy, charge densities, area/molecule and hydration energy have been calculated. The inhibition efficiency was calculated theoretically using the electronic parameters. From the obtained results, there is a significant difference between the inhibition efficiency of the electronic and the inhibition efficiency experimentally. The results were discussed on the light of the chemical structure of the used inhibitors. In general, the inhibition efficiency is affected by the shape and structure of the molecule.

  2. Faraday efficiency and mechanism of electrochemical surface reactions: CO2 reduction and H2 formation on Pt(111).

    Science.gov (United States)

    Hussain, Javed; Jónsson, Hannes; Skúlason, Egill

    2016-12-22

    An atomic scale model of the electrical double layer is used to calculate the mechanism and rate of electrochemical reduction of CO2 as well as H2 formation at a Pt(111) electrode. The water layer contains solvated protons and the electrode has excess electrons at the surface. Density functional theory within the generalized gradient approximation is used to describe the electronic structure while the mechanism and activation energy of the various elementary reactions is obtained by calculating minimum energy paths using the nudged elastic band method. The applied electrical potential is deduced from the calculated work function. The optimal reaction mechanism for CO2 reduction to either methane or methanol is found and the estimated rate compared with that of the competing reaction, H2 formation. When the free energy of only the intermediates and reactants is taken into account, not the activation energy, Pt(111) would seem to be a good electrocatalyst for CO2 reduction, significantly better than Cu(111). This, however, contradicts experimental findings. Detailed calculations reported here show that the activation energy for CO2 reduction is high for both Heyrovsky and Tafel mechanisms on Pt(111) in the relevant range of applied potential. The rate-limiting step of the Heyrovsky mechanism, *COOH + H+ + e- → *CO + H2O, is estimated to have an activation energy of 0.95 eV at -0.9 V vs. standard hydrogen electrode. Under the same conditions, the activation energy for H2 formation is estimated to be only 0.5 eV. This explains why attempts to reduce CO2 using platinum electrodes have produced only H2. A comparison is made with analogous results for Cu(111) [J. Hussain et al., Procedia Comput. Sci., 2015, 51, 1865] where a reaction mechanism with low activation energy for CO2 electroreduction to methane was identified. The difference between the two electrocatalysts is discussed.

  3. A highly sensitive BTX sensor based on electrochemically derived wall connected TiO{sub 2} nanotubes

    Energy Technology Data Exchange (ETDEWEB)

    Dutta, K. [Nano-Thin Films and Solid State Gas Sensor Devices Laboratory, Department of Electronics and Telecommunication Engineering, Indian Institute of Engineering Science and Technology, Shibpur, Howrah 711103 (India); Chattopadhyay, P.P. [Department of Metallurgy and Materials Engineering, Indian Institute of Engineering Science and Technology, Shibpur, Howrah 711103 (India); Lu, Chia-Wei [Graduate Institute of Photonics and Optoelectronics, National Taiwan University, Taipei 10617, Taiwan (China); Ho, Mon-Shu [Department of Physics, National Chung Hsing University, Taichung 40227, Taiwan (China); Bhattacharyya, P., E-mail: pb_etc_besu@yahoo.com [Nano-Thin Films and Solid State Gas Sensor Devices Laboratory, Department of Electronics and Telecommunication Engineering, Indian Institute of Engineering Science and Technology, Shibpur, Howrah 711103 (India)

    2015-11-01

    Highlights: • Electrochemically synthesized TiO{sub 2} nanotube array for sensing benzene, toluene, and xylene (BTX) with enhanced sensitivity at relatively low temperature is reported. • Structural characterizations (XRD, FESEM, and AFM), have revealed that variation of the H{sub 2}O concentrations in mixed electrolyte comprising ethylene glycol and ammonium fluoride (NH{sub 4}F + EG) resulted in the formation of four distinct TiO{sub 2} nanoforms. • Photo luminescence spectra (PL spectra) analysis has revealed distinctly different stoichiometry of the four anodized sample. • Among the various nanoforms, the wall connected TiO{sub 2} nanotube array has been found to be the most efficient one for BTX sensing in the concentration range 20–400 ppm at relatively lower operating temperature (50–200 °C). • Among the three target species, benzene was found to offer the highest response magnitude followed by toluene and xylene at all the concentrations. - Abstract: This paper concerns development of electrochemically synthesized titanium dioxide (TiO{sub 2}) nanotube array for sensing the carcinogenic aromatic hydrocarbons like benzene, toluene, and xylene (BTX) with enhanced sensitivity achievable at relatively low temperature. Structural characterizations (XRD, FESEM), revealed that variation of the H{sub 2}O concentrations (1%, 2%, 5%, 8%, 10%, and 100% by volume) in mixed electrolyte, comprising of ethylene glycol (EG) and ammonium fluoride (NH{sub 4}F), resulted in the formation of six distinctly different TiO{sub 2} nanoforms. Photo luminescence spectra (PL spectra) analysis authenticated different stoichiometry of these six samples. Besides, the X-ray photoelectron spectroscopy (XPS) was carried out to investigate the defect states. The XPS study enables to correlate the oxygen vacancy concentration with the anodization parameters. Among the various nanoforms, the wall connected TiO{sub 2} nanotube array was found to be the most efficient one for BTX

  4. Effects of low-pressure nitrogen plasma treatment on the surface properties and electrochemical performance of the polyethylene separator used lithium-ion batteries

    Science.gov (United States)

    Li, Chun; Li, Hsiao-Ling; Li, Chi-Heng; Liu, Yu-Shuan; Sung, Yu-Ching; Huang, Chun

    2018-01-01

    In this paper, we describe the surface transition of the polyethylene (PE) separator used in lithium-ion batteries treated by low-pressure nitrogen plasma discharge. The nitrogen-plasma-treated PE separator was characterized by contact angle measurement, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, and scanning electron microscopy. The electrochemical performance of the lithium ion batteries fabricated with the nitrogen-plasma-treated separator was also evaluated. Results showed that polar functionalization groups were induced on the PE surface by the nitrogen plasma discharge, causing the surface to become hydrophilic. The increases in surface wettability and surface free energy result in electrolyte retention improvement. Moreover, the nitrogen plasma-treated PE separator leads to superior performance in lithium-ion battery assembly.

  5. 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 ...

  6. A thermodynamical, electrochemical and surface investigation of Bis (indolyl methanes as Green corrosion inhibitors for mild steel in 1 M hydrochloric acid solution

    Directory of Open Access Journals (Sweden)

    Chandrabhan Verma

    2016-10-01

    Full Text Available The influence of three Bis (indolyl methanes (BIMs namely, 3,3′-((4-nitrophenyl methylene bis (1H-indole (BIM-1, 3,3′-(phenyl methylene bis (1H-indole (BIM-2 and 4-((1H-indol-2-yl(1H-indol-3-yl methyl phenol (BIM-3 on the mild steel corrosion in 1 M HCl was studied by weight loss, electrochemical, scanning electron microscopy (SEM, and dispersive X-ray spectroscopy (EDX methods. Results showed that BIM-3 shows maximum inhibition efficiency of 98.06% at 200 mg L−1 concentration. Polarization study revealed that the BIMs act as mixed type inhibitors. Adsorption of BIMs on the mild steel surface obeyed the Langmuir adsorption isotherm. The weight loss and electrochemical results were well supported by SEM and EDX studies.

  7. Electrospun lignin-derived carbon nanofiber mats surface-decorated with MnO2 nanowhiskers as binder-free supercapacitor electrodes with high performance

    Science.gov (United States)

    Ma, Xiaojing; Kolla, Praveen; Zhao, Yong; Smirnova, Alevtina L.; Fong, Hao

    2016-09-01

    The aim of this study is to explore innovative materials for the development of next-generation supercapacitor electrodes. The hypothesis is that, upon the surface-decoration with appropriate amount of MnO2 nanowhiskers, freestanding and highly graphitic electrospun carbon nanofiber (ECNF) mats (with fiber diameters of ∼200 nm and BET specific surface areas of ∼583 m2 g-1) derived from a natural product of lignin would be binder-free supercapacitor electrodes with high performance. To test the hypothesis, the ECNF mats have been prepared first; thereafter, the acquired ECNF mats have been surface-decorated with varied amounts of MnO2 nanowhiskers to prepare three types of ECNF/MnO2 mats. The morphological and structural properties of ECNF and ECNF/MnO2 mats are characterized by SEM, TEM and XRD, the weight percentages of MnO2 nanowhiskers in three ECNF/MnO2 mats are determined by thermal gravimetric analysis; while the electrochemical performance of each mat/electrode is evaluated by cyclic voltammetry, galvanostatic charge/discharge method, and electrochemical impedance spectroscopy. This study reveals that, all of the three ECNF/MnO2 mats/electrodes have significantly enhanced electrochemical performances compared to the ECNF mat/electrode; while the ECNF/MnO2 (1:1) mat/electrode exhibits the highest gravimetric capacitance of 83.3 F g-1, energy density of 84.3 W h kg-1, and power density of 5.72 kW kg-1.

  8. Performance improvements of alkaline batteries by studying the effects of different kinds of surfactant and different derivatives of benzene on the electrochemical properties of electrolytic zinc

    Science.gov (United States)

    Ghavami, Robab Khayat; Rafiei, Zahra

    Electrolytic zinc powders were prepared in 12 M KOH, 4 wt.% zinc oxide solutions in the presence of different kinds of surfactant and organic additives using the galvanostatic technique. Then the electrochemical behavior of zinc was investigated using the sweep voltametry technique. Zinc samples electrolyzed in the presence of cationic cetyl trimethyl ammonium bromide (Zn-CTAB), have maximum corrosion rate. Furthermore, scanning electron microscopy revealed the highest surface area. Zinc deposited with anionic surfactants, sodium dodecyl benzene sulfonate (SDBS) and sodium dodecyl sulfate (SDS), have high dendritic and secondary growth. More zinc ions electrolyzed on the cathode electrode in the presence of SDBS compared with SDS. We suppose the Benzene molecule in SDBS changes morphology, thus effects of the benzene molecule is investigated by utilizing several organic compounds during zinc electrodeposition. Naphthalene with 10 pi electrons at two fused rings decreases corrosion rate and needle growth of zinc deposited, compared to benzyl chloride which has 6 pi electrons. Enhanced delocalization of pi electrons by strongly activating group (-NH 2) in the aniline molecule increases the corrosion rate and dendrites compared with benzyl chloride, which has the weakly activating group (-CH 2Cl). The addition of chloro benzene with inactivating and electrodrawing group (-Cl) creates high surface area without any dendritic growth. The effects of electrolyte additives on the electrochemical capacity of AA-sized alkaline Zn-MnO 2 batteries are verified. The addition of Triton X-100 in anode gel resulted in maximum electrical capacity. Anionic (SDBS and SDS) additives gave higher electrical capacity than cationic (CTAB). Also, the reaction mechanism for zinc electrodeposition in alkaline electrolytes and its dependence upon the presence of organic additives are discussed in detail.

  9. Performance improvements of alkaline batteries by studying the effects of different kinds of surfactant and different derivatives of benzene on the electrochemical properties of electrolytic zinc

    Energy Technology Data Exchange (ETDEWEB)

    Ghavami, Robab Khayat; Rafiei, Zahra [Research & amp; Development Center, Niru Battery MFG. Co., P.O. Box 19575-361, Tehran (I.R. Iran)

    2006-11-22

    Electrolytic zinc powders were prepared in 12M KOH, 4wt.% zinc oxide solutions in the presence of different kinds of surfactant and organic additives using the galvanostatic technique. Then the electrochemical behavior of zinc was investigated using the sweep voltametry technique. Zinc samples electrolyzed in the presence of cationic cetyl trimethyl ammonium bromide (Zn-CTAB), have maximum corrosion rate. Furthermore, scanning electron microscopy revealed the highest surface area. Zinc deposited with anionic surfactants, sodium dodecyl benzene sulfonate (SDBS) and sodium dodecyl sulfate (SDS), have high dendritic and secondary growth. More zinc ions electrolyzed on the cathode electrode in the presence of SDBS compared with SDS. We suppose the Benzene molecule in SDBS changes morphology, thus effects of the benzene molecule is investigated by utilizing several organic compounds during zinc electrodeposition. Naphthalene with 10 pi electrons at two fused rings decreases corrosion rate and needle growth of zinc deposited, compared to benzyl chloride which has 6 pi electrons. Enhanced delocalization of pi electrons by strongly activating group (-NH{sub 2}) in the aniline molecule increases the corrosion rate and dendrites compared with benzyl chloride, which has the weakly activating group (-CH{sub 2}Cl). The addition of chloro benzene with inactivating and electrodrawing group (-Cl) creates high surface area without any dendritic growth. The effects of electrolyte additives on the electrochemical capacity of AA-sized alkaline Zn-MnO{sub 2} batteries are verified. The addition of Triton X-100 in anode gel resulted in maximum electrical capacity. Anionic (SDBS and SDS) additives gave higher electrical capacity than cationic (CTAB). Also, the reaction mechanism for zinc electrodeposition in alkaline electrolytes and its dependence upon the presence of organic additives are discussed in detail. (author)

  10. Influence of electrolytes (TEABF4 and TEMABF4) on electrochemical performance of graphite oxide derived from needle coke.

    Science.gov (United States)

    Yang, Sunhye; Kim, Ick-Jun; Choi, In-Sik; Bae, Mi-Kyeong; Kim, Hyun-Soo

    2013-05-01

    The structure of needle coke was changed to graphite oxide structure after oxidation treatment with 70 wt.% of nitric acid and sodium chlorate (NaClO3), and the inter-layer distance of the oxidized needle coke was expanded to 6.9 angstroms. The first charge profile of the oxidized needle coke-cell with 1.2 M TEMABF4/acetonitrile solution displayed that the intercalation of electrolyte ions into the inter-layer occurred at 1.0 V, which value is lower than 1.3 V of the oxidized needle coke-cell with 1.2 M TEABF4/acetonitrile solution. After first charge/discharge, the cell using TEMABF4 electrolyte exhibited smaller electrode resistance of 0.05 omega, and larger specific volume capacitance of 25.5 F/ml at the two-electrode system in the potential range 0-2.5 V than those of the cell using TEABF4 electrolyte. Compared to the TEABF4 electrolyte, better electrochemical performance of the TEMABF4 electrolyte in the oxidized needle coke may be caused by the smaller cation (TEMA+) size and better ion mobility in the nanopores between inter-layers.

  11. Metal (II) Complexes Derived from Naphthofuran-2-carbohydrazide and Diacetylmonoxime Schiff Base: Synthesis, Spectroscopic, Electrochemical, and Biological Investigation

    Science.gov (United States)

    Sumathi, R. B.; Halli, M. B.

    2014-01-01

    A new Schiff base and a new series of Co(II), Ni(II), Cu(II), Cd(II), and Hg(II) complexes were synthesized by the condensation of naphthofuran-2-carbohydrazide and diacetylmonoxime. Metal complexes of the Schiff base were prepared from their chloride salts of Co(II), Ni(II), Cu(II), Cd(II), and Hg(II) in ethanol. The ligand along with its metal complexes have been characterized on the basis of analytical data, IR, electronic, mass, 1HNMR, ESR spectral data, thermal studies, magnetic susceptibility, and molar conductance measurements. The nonelectrolytic behaviour of the complexes was assessed from the measured low conductance data. The elemental analysis of the complexes confirm the stoichiometry of the type CuL2Cl2 and MLCl2 where M = Ni(II), Co(II), Cd(II), and Hg(II) and L = Schiff base. The redox property of the Cu(II) complex was investigated by electrochemical method using cyclic voltammetry. In the light of these results, Co(II), Ni(II), and Cu(II) complexes are assigned octahedral geometry, Cd(II), and Hg(II) complexes tetrahedral geometry. In order to evaluate the effect of metal ions upon chelation, both the ligand and its metal complexes were screened for their antibacterial and antifungal activities by minimum inhibitory concentration (MIC) method. The DNA cleaving capacity of all the complexes was analysed by agarose gel electrophoresis method. PMID:24592203

  12. Synthesis and electrochemical, photophysical, and photochemical properties of ruthenium(II) 4,5-diazafluorenone complexes and their ketal derivatives

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Y.; Perez, W.; Zheng, G.Y.; Rillema, D.P. [Wichita State Univ., KS (United States). Dept. of Chemistry

    1998-04-20

    A series of ruthenium(II) complexes of the types [Ru(bpy){sub n}(dafo){sub 3{minus}n}]{sup 2+} and [Ru(bpy){sub n}(dafo-ketal){sub 3{minus}n}]{sup 2+}, where n varies between 0 and 3 and dafo is 4,5-diazafluoren-9-one, were synthesized, and their chemical, physical, and photophysical properties were examined. The coordinated dafo-ketal ligand readily forms by the direct reaction of [Ru(bpy){sub n}(dafo){sub 3{minus}n}]{sup 2+} complexes with ethylene glycol or by reaction of the appropriate ruthenium precursors with the correct stoichiometric amount of he dafo ligand in ethylene glycol. In each series, the visible absorption band associated with the MLCT transition shifts to the blue and the electrochemical oxidation associated with the Ru(III)/Ru(II) couple becomes more positive as n decreases. Coordinated dafo undergoes a one-electron reduction at potentials < {minus}1 V and a second one-electron reduction at {approximately} {minus}1.2 V vs SSCE. The first reduction can be associated with reduction of the carbonyl group; the second, with reduction of the bipyridine portion. Coordinated dafo-ketal only reduces at potentials < {minus}1.2 V. The emission properties place the emitting state of the complexes on the bipyridine portion of the dafo ligand, not the carbonyl group. At 77 K in a 4:1 ethanol-methanol glass, the emission lifetimes fall in a range of 5--2 {micro}s as n decreases. In fluid solution, the emission lifetimes are temperature dependent with activation energies that vary from 1,400 to 500 cm{sup {minus}1} as n decreases. The thermally accessible state is assigned as a fourth metal-to-ligand charge transfer (MLCT{double_prime}) state since the compounds are photochemically unreactive.

  13. Synthesis, electrochemical, spectrophotometric and potentiometric studies of two azo-compounds derived from 4-amino-2-methylquinoline in ethanolic-aqueous buffered solutions

    Energy Technology Data Exchange (ETDEWEB)

    El-Attar, Mona A.; Ghoneim, Mohamed M. [Analytical Chemistry Research Unit, Chemistry Department, Tanta University (Egypt); Ismail, Iqbal M., E-mail: maema.2011@yahoo.com [Chemistry Department, Faculty of Science, King Abdul Aziz University, Jeddah (Saudi Arabia)

    2012-08-15

    Two azo-compounds, 2-methyl-4-(5-amino-2-hydroxy-phenylazo)-quinoline (2) and 2-methyl-4-(2-hydroxy-5-nitrophenylazo)-quinoline, derived from 4-amino-2-methylquinoline were synthesized. Their chemical structures were characterized and confirmed by means of elemental chemical analysis, infrared (IR) spectroscopy, {sup 1}H nuclear magnetic resonance (NMR) and mass spectrometry (MS). The electrochemical behavior of the starting compound (4-amino-2-methylquinoline) and of the two synthesized azo-derivatives was studied at the mercury electrode in the B-R universal buffer at various pH values (2-11.5) containing 40% (v/v) ethanol using dc-polarography, cyclic voltammetry and controlled-potential coulometry. Their electrode reaction pathways were elucidated and discussed. The dissociation constants (pKa) of the examined compounds, stability constants and stoichiometry of their complexes in solution with some transition metal ions (Co(II), Ni(II), Cu(II), La(III) and UO{sup 2+}{sub 2}) were determined. (author)

  14. Regional trends in surface solar radiation derived from satellite-based data sets

    Science.gov (United States)

    Trentmann, Jörg; Sanchez-Lorenzo, Arturo; Posselt, Rebekka; Krähenmann, Stefan; Müller, Richard W.; Wild, Martin; Stöckli, Reto; Ahrens, Bodo

    2013-04-01

    The monitoring of the surface solar radiation and the detection of its variability and possible changes is highly relevant for our understanding of the climate system. Clouds and aerosols are the main contributors to the observed changes in the solar energy reaching the surface. Clouds are well observed from satellites, especially during daytime, making satellite-derived data sets of the surface radiation a potentially powerful source of information to assess the spatial structure of surface solar radiation. Surface-based observations, e.g., from the BSRN and GEBA networks, have been used to assess the temporal variability and trend of the surface radiation. Due to the limited spatial distribution of the surface stations, a generalization of the trends derived from measurements at individual stations is difficult. Satellite-derived data of the surface radiation, providing up to global coverage, are available since the 1980s allowing an analysis of the regional variability of temporal changes of the surface radiation. Here, we use surface solar radiation data generated and provided by the EUMETSAT Satellite Application Facility on Climate Monitoring (CM SAF, www.cmsaf.eu) based on geostationary and polar-orbiting satellites. The ability of the satellite-derived data sets to detect trends is tested and assessed by comparison with surface reference observations in Europe. It is shown that, at least for part of the available time series, the satellite data is stable and can be used to derive trend estimates. Substantial regional differences in the trend of the surface solar radiation are detected across Europe between 1994 and 2005, with strong positive trends over Central Europe (brightening) and negative trends over the Mediterranean Sea (dimming).

  15. Study of fibrinogen adsorption on hydroxyapatite and TiO2 surfaces by electrochemical piezoelectric quartz crystal impedance and FTIR-ATR spectroscopy.

    Science.gov (United States)

    Yang, Qin; Zhang, Youyu; Liu, Meiling; Ye, Min; Zhang, YuQin; Yao, Shouzhuo

    2007-07-30

    The electrochemical piezoelectric quartz crystal impedance (EQCI), a combined technique of piezoelectric quartz crystal impedance (PQCI), electrochemical impedance (EI), and Fourier transform infrared spectroscopy-attenuated total internal reflectance spectroscopy (FTIR-ATR) were used to in situ study the adsorption process of fibrinogen onto the surface of biomaterials-TiO2 and hydroxyapatite (Ca5(PO4)3OH, HAP). The equivalent circuit parameters, the resonance frequencies and the half peak width of the conductance spectrum of the two biomaterial-modified piezoelectric quartz crystal (PQC) resonances as well as the FTIR-ATR spectra of fibrinogen during fibrinogen adsorption on TiO2 and HAP particles modified electrode surface were obtained. The adsorption kinetics and mechanism of fibrinogen were investigated and discussed as well. The results suggested that two consecutive steps occurred during the adsorption of fibrinogen onto TiO2 and hydroxyapatite (HAP) surface. The fibrinogen molecules were firstly adsorbed onto the surface, and then the rearrangement of adsorbed fibrinogen or multi-layered adsorption occurred. The FTIR-ATR spectroscopy investigations showed that the secondary structure of fibrinogen molecules was altered during the adsorption and the adsorption kinetics of fibrinogen related with the variety of biomaterials. These experimental results suggest a way for enriching biological analytical science and developing new applications of analytical techniques, such as PQCI, EI, and FTIR-ATR.

  16. In situ electrochemical-transmission surface plasmon resonance spectroscopy for poly(pyrrole-3-carboxylic acid) thin-film-based biosensor applications.

    Science.gov (United States)

    Janmanee, Rapiphun; Baba, Akira; Phanichphant, Sukon; Sriwichai, Saengrawee; Shinbo, Kazunari; Kato, Keizo; Kaneko, Futao

    2012-08-01

    In this study, we describe the combination of transmission surface plasmon resonance (TSPR) and electrochemical techniques for the application to biosensors with conducting polymers. Electropolymerization was employed to construct poly(pyrrole-3-carboxylic acid) (PP3C) film on a gold-coated grating substrate using pyrrole-3-carboxylic acid (P3C) monomer solution in 0.5 M H(2)SO(4). In situ electrochemical-transmission surface plasmon resonance (EC-TSPR) measurements were carried out to study the kinetic and electroactivity properties of PP3C film. Immobilization of antihuman IgG on the activated surface and the binding process of human IgG and antihuman IgG in neutral solution could be detected in situ by EC-TSPR measurement. The surface modification steps on the PP3C layer led to an increase in intensity of the transmission peak. The performance, sensitivity, and utility of EC-TSPR spectroscopy showed obvious advantages for the detection of binding process with the simple experimental setup, and could be applied to the study of biomolecular interactions in various systems.

  17. Evaluation of chemically modified Ti–5Mo–3Fe alloy surface: Electrochemical aspects and in vitro bioactivity on MG63 cells

    Energy Technology Data Exchange (ETDEWEB)

    Kumar, A. Madhan [Center of Research Excellence in Corrosion, King Fahd University of Petroleum and Minerals, Dhahran 31261 (Saudi Arabia); Sudhagar, P. [Energy Materials Laboratory, WCU Program Department of Energy Engineering, Hanyang University, Seoul 133-791 (Korea, Republic of); Ramakrishna, Suresh [Graduate School of Biomedical Science and Engineering/College of Medicine, Hanyang University, Sungdong-gu, Seoul (Korea, Republic of); Kang, Yong Soo [Energy Materials Laboratory, WCU Program Department of Energy Engineering, Hanyang University, Seoul 133-791 (Korea, Republic of); Kim, Hyongbum [Graduate School of Biomedical Science and Engineering/College of Medicine, Hanyang University, Sungdong-gu, Seoul (Korea, Republic of); Gasem, Zuhair M. [Center of Research Excellence in Corrosion, King Fahd University of Petroleum and Minerals, Dhahran 31261 (Saudi Arabia); Rajendran, N., E-mail: nrajendran@annauniv.edu [Department of Chemistry, Anna University, Chennai (India)

    2014-07-01

    Ti–5Mo–3Fe (TMF) alloy is a newly developed β-titanium alloy with low modulus, and it has been deemed as suitable material for dental or orthopaedic implant. The aim of the present study is to evaluate the effect of alkali and hydrogen peroxide treatment on the corrosion and biological performance of TMF surface. The phases, morphology with chemical composition and topography of the treated surface were examined by X-ray diffraction, scanning electron microscopy (SEM) coupled with energy dispersive X-ray (EDAX) analysis and atomic force microscopy (AFM), respectively. Micro hardness of treated substrates was measured using Vicker's micro hardness method. The electrochemical studies were carried out using potentiodynamic polarisation and electrochemical impedance spectroscopy (EIS) measurements. In order to describe the bio-activity, contact angle measurements, in vitro characterisation and cell culture studies were performed for treated TMF surfaces in simulated body fluid (SBF) and MG63 cells. All these observations showed that the NaOH treatment is the most appropriate method for TMF alloy which exhibited superior biocompatibility and enhanced corrosion protection performance due to their hydrophilic, smooth, compact porous surface morphology than that of other substrates.

  18. NATO Advanced Research Workshop on Geometrical Derivatives of Energy Surfaces and Molecular Properties

    CERN Document Server

    Simons, Jack

    1986-01-01

    The development and computational implementation of analytical expres­ sions for the low-order derivatives of electronic energy surfaces and other molecular properties has undergone rapid growth in recent years. It is now fairly routine for chemists to make use of energy gradient information in locating and identifying stable geometries and transition states. The use of second analytical derivative (Hessian or curvature) expressions is not yet routine, and third and higher energy derivatives as well as property (e.g., dipole moment, polarizability) derivatives are just beginning to be applied to chemical problems. This NATO Advanced Research Workshop focused on analyzing the re­ lative merits of various strategies for deriving the requisite analyti­ cal expressions, for computing necessary integral derivatives and wave­ function parameter derivatives, and for efficiently coding these expres­ sions on conventional scalar machines and vector-oriented computers. The participant list contained many scientist...

  19. Mercapto-ordered carbohydrate-derived porous carbon electrode as a novel electrochemical sensor for simple and sensitive ultra-trace detection of omeprazole in biological samples.

    Science.gov (United States)

    Kalate Bojdi, Majid; Behbahani, Mohammad; Mashhadizadeh, Mohammad Hosein; Bagheri, Akbar; Hosseiny Davarani, Saied Saeed; Farahani, Ali

    2015-03-01

    We are introducing mercapto-mesoporous carbon modified carbon paste electrode (mercapto-MP-C-CPE) as a new sensor for trace determination of omeprazole (OM) in biological samples. The synthesized modifier was characterized by thermogravimetry analysis (TGA), differential thermal analysis (DTA), transmission electron microscopy (TEM), Fourier transform infrared spectrometry (FT-IR), X-ray diffraction (XRD), elemental analysis (CHN) and N2 adsorption surface area measurement (BET). The electrochemical response characteristic of the modified-CPE toward OM was investigated by cyclic and differential pulse voltammetry (CV and DPV). The proposed sensor displayed a good electrooxidation response to the OM, its linear range is 0.25nM to 25μM with a detection limit of 0.04nM under the optimized conditions. The prepared modified electrode shows several advantages such as high sensitivity, long-time stability, wide linear range, ease of preparation and regeneration of the electrode surface by simple polishing and excellent reproducibility. Copyright © 2014 Elsevier B.V. All rights reserved.

  20. Mercapto-ordered carbohydrate-derived porous carbon electrode as a novel electrochemical sensor for simple and sensitive ultra-trace detection of omeprazole in biological samples

    Energy Technology Data Exchange (ETDEWEB)

    Kalate Bojdi, Majid [Department of Chemistry, Faculty of Science, Shahid Beheshti University, Tehran 1983963113 (Iran, Islamic Republic of); Faculty of Chemistry, Kharazmi (Tarbiat Moallem) University, Tehran (Iran, Islamic Republic of); Behbahani, Mohammad [Department of Chemistry, Faculty of Science, Shahid Beheshti University, Tehran 1983963113 (Iran, Islamic Republic of); Mashhadizadeh, Mohammad Hosein [Faculty of Chemistry, Kharazmi (Tarbiat Moallem) University, Tehran (Iran, Islamic Republic of); Bagheri, Akbar [Department of Chemistry, Faculty of Science, Shahid Beheshti University, Tehran 1983963113 (Iran, Islamic Republic of); Hosseiny Davarani, Saied Saeed, E-mail: ss-hosseiny@sbu.ac.ir [Department of Chemistry, Faculty of Science, Shahid Beheshti University, Tehran 1983963113 (Iran, Islamic Republic of); Farahani, Ali [Department of Chemistry, Faculty of Science, Shahid Beheshti University, Tehran 1983963113 (Iran, Islamic Republic of)

    2015-03-01

    We are introducing mercapto-mesoporous carbon modified carbon paste electrode (mercapto-MP-C-CPE) as a new sensor for trace determination of omeprazole (OM) in biological samples. The synthesized modifier was characterized by thermogravimetry analysis (TGA), differential thermal analysis (DTA), transmission electron microscopy (TEM), Fourier transform infrared spectrometry (FT-IR), X-ray diffraction (XRD), elemental analysis (CHN) and N{sub 2} adsorption surface area measurement (BET). The electrochemical response characteristic of the modified-CPE toward OM was investigated by cyclic and differential pulse voltammetry (CV and DPV). The proposed sensor displayed a good electrooxidation response to the OM, its linear range is 0.25 nM to 25 μM with a detection limit of 0.04 nM under the optimized conditions. The prepared modified electrode shows several advantages such as high sensitivity, long-time stability, wide linear range, ease of preparation and regeneration of the electrode surface by simple polishing and excellent reproducibility. - Highlights: • A modified nanoporous carbon as a novel sensor • High stability and good repeatability and reproducibility by the prepared sensor • Trace determination of omeprazole • Biological and pharmaceutical samples.

  1. Carbon xerogel microspheres and monoliths from resorcinol-formaldehyde mixtures with varying dilution ratios: preparation, surface characteristics, and electrochemical double-layer capacitances.

    Science.gov (United States)

    Zapata-Benabithe, Zulamita; Carrasco-Marín, Francisco; de Vicente, Juan; Moreno-Castilla, Carlos

    2013-05-21

    Carbon xerogels in the form of microspheres and monoliths were obtained from the sol-gel polymerization of resorcinol and formaldehyde in the presence of potassium carbonate as catalyst, using water as solvent and two different molar dilution ratios. The objectives of this study were as follows: to investigate the effect of the dilution ratio, polymerization reaction time, and temperature on the rheological properties of the sols used to prepare the carbon xerogel microspheres and monoliths; and to determine the influence of their preparation methods and shapes on their surface characteristics and electrochemical double-layer (EDL) capacitance. An increase in the molar dilution ratio produced a decrease in the apparent activation energy of the sol-gel transition. Carbon xerogel microspheres were steam-activated at different burnoff percentages. The morphology, surface area, porosity, and surface chemistry of samples were determined. The main difference between the carbon xerogel microspheres and monoliths was that the latter are largely mesoporous. Better electrochemical behavior was shown by carbon xerogels in monolith than in microsphere form, but higher gravimetric and volumetric capacitances were found in activated carbon xerogel microspheres than in carbon xerogel monoliths.

  2. The Surface Coating of Commercial LiFePO4 by Utilizing ZIF-8 for High Electrochemical Performance Lithium Ion Battery

    Science.gov (United States)

    Xu, XiaoLong; Qi, CongYu; Hao, ZhenDong; Wang, Hao; Jiu, JinTing; Liu, JingBing; Yan, Hui; Suganuma, Katsuaki

    2018-03-01

    The requirement of energy-storage equipment needs to develop the lithium ion battery (LIB) with high electrochemical performance. The surface modification of commercial LiFePO4 (LFP) by utilizing zeolitic imidazolate frameworks-8 (ZIF-8) offers new possibilities for commercial LFP with high electrochemical performances. In this work, the carbonized ZIF-8 (CZIF-8) was coated on the surface of LFP particles by the in situ growth and carbonization of ZIF-8. Transmission electron microscopy indicates that there is an approximate 10 nm coating layer with metal zinc and graphite-like carbon on the surface of LFP/CZIF-8 sample. The N2 adsorption and desorption isotherm suggests that the coating layer has uniform and simple connecting mesopores. As cathode material, LFP/CZIF-8 cathode-active material delivers a discharge specific capacity of 159.3 mAh g-1 at 0.1C and a discharge specific energy of 141.7 mWh g-1 after 200 cycles at 5.0C (the retention rate is approximate 99%). These results are attributed to the synergy improvement of the conductivity, the lithium ion diffusion coefficient, and the degree of freedom for volume change of LFP/CZIF-8 cathode. This work will contribute to the improvement of the cathode materials of commercial LIB.[Figure not available: see fulltext.

  3. Oriented Immobilization of His-Tagged Protein on a Redox Active Thiol Derivative of DPTA-Cu(II Layer Deposited on a Gold Electrode—The Base of Electrochemical Biosensors

    Directory of Open Access Journals (Sweden)

    Hanna Radecka

    2013-09-01

    Full Text Available This paper concerns the development of an electrochemical biosensor for the determination of Aβ16–23' and Aβ1–40 peptides. The His-tagged V and VC1 domains of Receptor for Advanced Glycation end Products (RAGE immobilized on a gold electrode surface were used as analytically active molecules. The immobilization of His6–RAGE domains consists of: (i formation of a mixed layer of N-acetylcysteamine (NAC and the thiol derivative of pentetic acid (DPTA; (ii complexation of Cu(II by DPTA; (iii oriented immobilization of His6–RAGE domains via coordination bonds between Cu(II sites from DPTA–Cu(II complex and imidazole nitrogen atoms of a histidine tag. Each modification step was controlled by cyclic voltammetry (CV, Osteryoung square-wave voltammetry (OSWV, and atomic force microscopy (AFM. The applicability of the proposed biosensor was tested in the presence of human plasma, which had no influence on its performance. The detection limits for Aβ1–40 determination were 1.06 nM and 0.80 nM, in the presence of buffer and human plasma, respectively. These values reach the concentration level of Aβ1–40 which is relevant for determination of its soluble form in human plasma, as well as in brain. This indicates the promising future application of biosensor presented for early diagnosis of neurodegenerative diseases.

  4. Synthesis, spectroscopic, electrochemical and computational studies of rhenium(i) tricarbonyl complexes based on bidentate-coordinated 2,6-di(thiazol-2-yl)pyridine derivatives.

    Science.gov (United States)

    Klemens, Tomasz; Czerwińska, Katarzyna; Szlapa-Kula, Agata; Kula, Slawomir; Switlicka, Anna; Kotowicz, Sonia; Siwy, Mariola; Bednarczyk, Katarzyna; Krompiec, Stanisław; Smolarek, Karolina; Maćkowski, Sebastian; Danikiewicz, Witold; Schab-Balcerzak, Ewa; Machura, Barbara

    2017-07-25

    Nine rhenium(i) complexes possessing three carbonyl groups together with a bidentate coordinated 2,6-di(thiazol-2-yl)pyridine derivative were synthesized to examine the impact of structure modification of the triimine ligand on the photophysical, thermal and electrochemical properties of [ReCl(CO)3(4-R(n)-dtpy-κ(2)N)]. The Re(i) complexes were fully characterized using IR, (1)H and (13)C, HRMS-ESI and single crystal X-ray analysis. Their thermal properties were evaluated using DSC and TGA measurements. Photoluminescence spectra of [ReCl(CO)3(4-R(n)-dtpy-κ(2)N)] were investigated in solution and in the solid state, at 298 and 77 K. Both emission wavelengths and quantum yields of [ReCl(CO)3(4-R(n)-dtpy-κ(2)N)] were found to be structure-related, demonstrating a crucial role of the substituent attached to the 2,6-di(thiazol-2-yl)pyridine skeleton. In order to fully understand the photophysical properties of [ReCl(CO)3(4-R(n)-dtpy-κ(2)N)], density functional theory (DFT) and time-dependent DFT (TD-DFT) calculations were performed. Furthermore, the complexes which showed appropriate solubility in chloroform were tested as an emissive active layer in OLED devices.

  5. Synthesis, structural characterization, electrochemical and biological studies on divalent metal chelates of a new ligand derived from pharmaceutical preservative, dehydroacetic acid, with 1,4-diaminobenzene

    Directory of Open Access Journals (Sweden)

    Sanaa M. Emam

    2017-05-01

    Full Text Available Cobalt(II, nickel(II, copper(II, zinc(II and cadmium(II complexes of new 3-acetyl-4-[(4-aminophenylamino]-6-methyl-2H-pyran-2-one (HL1 derived from dehydroacetic acid and 1,4-diaminobenzene were prepared and characterized. The structural features were determined from their elemental analyses, 1H, and 13C-NMR spectra, molar conductivities, magnetic moments, IR, UVvis. spectra, thermal analyses (D.T.A. and T.G.A. and E.S.R. measurements. Their magnetic susceptibility measurements and low conductance data provide evidence for the mono- or dimeric and non-electrolytic nature of the solid complexes. The E.S.R. spectra of copper(II complexes show axial type symmetry with covalent or ionic bond character. The electrochemical behavior of the complexes in DMF (dimethylformamide solvent at 298 K was studied. The biological activity of the ligand and its metal(II complexes was also studied. The obtained complexes showed higher activities than the free ligand in protecting the Egyptian cotton fields from Spodoptera littoralis larvae.

  6. Molecular association of 2-(n-alkylamino)-1,4-naphthoquinone derivatives: Electrochemical, DFT studies and antiproliferative activity against leukemia cell lines

    Science.gov (United States)

    Patil, Rishikesh; Bhand, Sujit; Konkimalla, V. Badireenath; Banerjee, Priyabrata; Ugale, Bharat; Chadar, Dattatray; Saha, Sourav Kr.; Praharaj, Prakash Priyadarshi; Nagaraja, C. M.; Chakrovarty, Debamitra; Salunke-Gawali, Sunita

    2016-12-01

    Molecular structures and their molecular association of 2-(n-alkylamino)-1,4-naphthoquinone, viz., LH-3; propyl, LH-4; butyl and LH-8; octyl derivatives were studied by single crystal X-ray diffraction studies. Synthesis and characterization of 2-octylamino-1,4-naphthoquinone; LH-8 was discussed. The molecule of LH-3 crystallizes in orthorhombic space group P21/c, while the LH-4 and LH-8 molecule crystallizes in triclinic space group P-1. LH-3, LH-4 and LH-8 showed intermolecular N-H⋯O and C-H⋯O interactions, LH-3 showed unique C(3)-H(3)⋯O(1) interaction. Interchain π-π stacking, slipped π-π stacking and C⋯O close contacts was respectively observed in LH-3, LH-4 and LH-8. Electrochemical studies were performed on first eight members of homologous series of 2-(n-alkylamino)-1,4-naphthoquinone (LH-1 to LH-8) by cyclic voltammetry. Naphthoquinone to naphthosemiquinone reversible redox couple was observed in all compounds ∼ E1/2 = -0.657 ± 0.05 V. HOMO-LUMO band gap was determined for the neutral form as well as the monoanionic radical form viz. naphthosemiquinone form of selected derivatives by DFT studies. It has been observed that the electron density is delocalized in the naphthoquinone ring in both neutral as well as one electron reduced form of compounds. Antiproliferative activity of LH-1 to LH-8 was evaluated against two cancer cell lines, THP1(acute monocytic leukemia) and K562(human immortalized myelogenous leukemia cell line) cells. It was observed that, in THP1 cells, compounds LH-2 and LH-3 are very active while LH-1, LH-4 and LH-6 were moderately active and LH-5, LH-7 and LH-8 were totally inactive. Contrastingly, in K562 cells all of the compounds were moderately active.

  7. Investigation of possibility of surface rupture derived from PFDHA and calculation of surface displacement based on dislocation

    Science.gov (United States)

    Inoue, N.; Kitada, N.; Irikura, K.

    2013-12-01

    A probability of surface rupture is important to configure the seismic source, such as area sources or fault models, for a seismic hazard evaluation. In Japan, Takemura (1998) estimated the probability based on the historical earthquake data. Kagawa et al. (2004) evaluated the probability based on a numerical simulation of surface displacements. The estimated probability indicates a sigmoid curve and increases between Mj (the local magnitude defined and calculated by Japan Meteorological Agency) =6.5 and Mj=7.0. The probability of surface rupture is also used in a probabilistic fault displacement analysis (PFDHA). The probability is determined from the collected earthquake catalog, which were classified into two categories: with surface rupture or without surface rupture. The logistic regression is performed for the classified earthquake data. Youngs et al. (2003), Ross and Moss (2011) and Petersen et al. (2011) indicate the logistic curves of the probability of surface rupture by normal, reverse and strike-slip faults, respectively. Takao et al. (2013) shows the logistic curve derived from only Japanese earthquake data. The Japanese probability curve shows the sharply increasing in narrow magnitude range by comparison with other curves. In this study, we estimated the probability of surface rupture applying the logistic analysis to the surface displacement derived from a surface displacement calculation. A source fault was defined in according to the procedure of Kagawa et al. (2004), which determined a seismic moment from a magnitude and estimated the area size of the asperity and the amount of slip. Strike slip and reverse faults were considered as source faults. We applied Wang et al. (2003) for calculations. The surface displacements with defined source faults were calculated by varying the depth of the fault. A threshold value as 5cm of surface displacement was used to evaluate whether a surface rupture reach or do not reach to the surface. We carried out the

  8. Reaction pathways of model compounds of biomass-derived oxygenates on Fe/Ni bimetallic surfaces

    Science.gov (United States)

    Yu, Weiting; Chen, Jingguang G.

    2015-10-01

    Controlling the activity and selectivity of converting biomass-derivatives to fuels and valuable chemicals is critical for the utilization of biomass feedstocks. There are primarily three classes of non-food competing biomass, cellulose, hemicellulose and lignin. In the current work, glycolaldehyde, furfural and acetaldehyde are studied as model compounds of the three classes of biomass-derivatives. Monometallic Ni(111) and monolayer (ML) Fe/Ni(111) bimetallic surfaces are studied for the reaction pathways of the three biomass surrogates. The ML Fe/Ni(111) surface is identified as an efficient surface for the conversion of biomass-derivatives from the combined results of density functional theory (DFT) calculations and temperature programmed desorption (TPD) experiments. A correlation is also established between the optimized adsorption geometry and experimental reaction pathways. These results should provide helpful insights in catalyst design for the upgrading and conversion of biomass.

  9. Preparation of nitrogen-doped cotton stalk microporous activated carbon fiber electrodes with different surface area from hexamethylenetetramine-modified cotton stalk for electrochemical degradation of methylene blue

    Science.gov (United States)

    Li, Kunquan; Rong, Zhang; Li, Ye; Li, Cheng; Zheng, Zheng

    Cotton-stalk activated carbon fibers (CSCFs) with controllable micropore area and nitrogen content were prepared as an efficient electrode from hexamethylenetetramine-modified cotton stalk by steam/ammonia activation. The influence of microporous area, nitrogen content, voltage and initial concentration on the electrical degradation efficiency of methylene blue (MB) was evaluated by using CSCFs as anode. Results showed that the CSCF electrodes exhibited excellent MB electrochemical degradation ability including decolorization and COD removal. Increasing micropore surface area and nitrogen content of CSCF anode leaded to a corresponding increase in MB removal. The prepared CSCF-800-15-N, which has highest N content but lowest microporous area, attained the best degradation effect with 97% MB decolorization ratio for 5 mg/L MB at 12 V in 4 h, implying the doped nitrogen played a prominent role in improving the electrochemical degradation ability. The electrical degradation reaction was well described by first-order kinetics model. Overall, the aforesaid findings suggested that the nitrogen-doped CSCFs were potential electrode materials, and their electrical degradation abilities could be effectively enhanced by controlling the nitrogen content and micropore surface area.

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

    Science.gov (United States)

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

    2005-09-01

    A composite of Ti-V-based bcc phase alloy surface-modified with AB5 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 +10wt%AB5 showed a discharge capacity in the first cycle, at 353 K, of 886mAhg-1, corresponding to 3.38 wt % of hydrogen, with a 45mAg-1 discharge current. It is thought that this high capacity is due to the enhanced electrochemical-catalytic activity from the alloy surface covered with AB5 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.

  11. METHOD FOR ELECTROCHEMICAL PHOSPHATING OF METAL SURFACES, PARTICULARLY STAINLESS STEEL, AND APPLICATION OF AN AQUEOUS PHOSPHATING SOLUTION FOR SUCH A METHOD

    DEFF Research Database (Denmark)

    1998-01-01

    A method for electrochemical phosphating of metal surfaces, particularly stainless steel, in connection with cold forming of metal workpieces, which method provides the cold formed work-piece with a lubricant after phosphating, involves an electrochemical phosphating through a cathodic process...... applying an aqueous phosphating solution containing: 0.5 to 100 g Ca?2+¿/1, 0.5 to 100 g Zn?2+¿/1, 5 to 100 g PO¿4??3-¿/1, 0 to 100 g NO¿3??-¿/1, 0 to 100 g ClO¿3??-¿/1 and 0 to 50 g F?-¿ or Cl?-¿/1, by which the temperature of the solution is between 0 and 95 °C, the pH-value of the solution is between 0.......5 and 5, and the current density is between 0.1 and 250 mA/cm?2¿. This gives a good lubrication effect, a good adhesion to the metal surface, particularly stainless steel, and a more expedient texture than ordinary phosphating....

  12. Heteroatom-enriched and renewable banana-stem-derived porous carbon for the electrochemical determination of nitrite in various water samples

    Science.gov (United States)

    Madhu, Rajesh; Veeramani, Vediyappan; Chen, Shen-Ming

    2014-04-01

    For the first time, high-surface-area (approximately 1465 m2 g-1), highly porous and heteroatom-enriched activated carbon (HAC) was prepared from banana stems (Musa paradisiaca, Family: Musaceae) at different carbonization temperatures of 700, 800 and 900°C (HAC) using a simple and eco-friendly method. The amounts of carbon, hydrogen, nitrogen and sulfur in the HAC are 61.12, 2.567, 0.4315, and 0.349%, respectively. Using X-ray diffraction (XRD), CHNS elemental analysis, X-ray photoelectron spectroscopy (XPS) and Raman spectroscopy, the prepared activated carbon appears amorphous and disordered in nature. Here, we used HAC for an electrochemical application of nitrite (NO2-) sensor to control the environmental pollution. In addition, HAC exhibits noteworthy performance for the highly sensitive determination of nitrite. The limit of detection (LODs) of the nitrite sensor at HAC-modified GCE is 0.07 μM. In addition, the proposed method was applied to determine nitrite in various water samples with acceptable results.

  13. Cellular Behavior of Human Adipose-Derived Stem Cells on Wettable Gradient Polyethylene Surfaces

    Directory of Open Access Journals (Sweden)

    Hyun Hee Ahn

    2014-01-01

    Full Text Available Appropriate surface wettability and roughness of biomaterials is an important factor in cell attachment and proliferation. In this study, we investigated the correlation between surface wettability and roughness, and biological response in human adipose-derived stem cells (hADSCs. We prepared wettable and rough gradient polyethylene (PE surfaces by increasing the power of a radio frequency corona discharge apparatus with knife-type electrodes over a moving sample bed. The PE changed gradually from hydrophobic and smooth surfaces to hydrophilic (water contact angle, 90° to ~50° and rough (80 to ~120 nm surfaces as the power increased. We found that hADSCs adhered better to highly hydrophilic and rough surfaces and showed broadly stretched morphology compared with that on hydrophobic and smooth surfaces. The proliferation of hADSCs on hydrophilic and rough surfaces was also higher than that on hydrophobic and smooth surfaces. Furthermore, integrin beta 1 gene expression, an indicator of attachment, and heat shock protein 70 gene expression were high on hydrophobic and smooth surfaces. These results indicate that the cellular behavior of hADSCs on gradient surface depends on surface properties, wettability and roughness.

  14. Electropolishing of stainless steels in a choline chloride based ionic liquid: an electrochemical study with surface characterisation using SEM and atomic force microscopy.

    Science.gov (United States)

    Abbott, Andrew P; Capper, Glen; McKenzie, Katy J; Glidle, Andrew; Ryder, Karl S

    2006-09-28

    We have studied the anodic dissolution (electropolishing) of various stainless steel alloys in an ionic liquid comprising a 2 : 1 stoichiometric mix of ethylene glycol (EG) and choline chloride. We have used a combination of electrochemical and spectroscopic methods together with in situ liquid probe microscopy. We discuss the role and influence of the surface oxide passivation layer, characterized here by X-ray photoelectron spectroscopy (XPS) and linear sweep voltammetry, on the polishing process. We address the question of dealloying during the polish in order to contribute to our understanding of the viability of the ionic liquid as a replacement industrial electropolishing medium; the current commercial process uses a corrosive mixture of phosphoric and sulfuric acids. Also, we present data from ex situ and in situ liquid AFM studies giving both a qualitative and quantitative insight into the nature and scale of morphological changes at the steel surface during the polishing process.

  15. Measurement of surface resistivity/conductivity of different organic thin films by a combination of optical shearography and electrochemical impedance spectroscopy

    Science.gov (United States)

    Habib, Khaled

    2013-11-01

    Shearography techniques were applied again to measure the surface resistivity/conductivity of different organic thin films on a metallic substrate. The coatings were ACE premium-grey enamel (spray coating), a yellow Acrylic lacquer, and a gold nail polish on a carbon steel substrate. The investigation was focused on determining the in-plane displacement of the coatings by shearography between 20 and 60 °C. Then, the alternating current (AC) impedance (resistance) of the same coated samples was determined by electrochemical impedance spectroscopy (EIS) in 3.0% NaCl solution at room temperature. As a result, the proportionality constant (resistivity or conductivity = 1/surface resistivity) between the determined AC impedance and the in-plane displacement was obtained. The obtained resistivity of all investigated coatings, 40:15 × 106-24:6 × 109Ωcm, was found in the insulator range.

  16. A novel ferrocenic copper(II) complex Salen-like, derived from 5-chloromethyl-2-hydroxyacetophenone and N-ferrocenmethylaniline: Design, spectral approach and solvent effect towards electrochemical behavior of Fc+/Fc redox couple

    OpenAIRE

    Ouennoughi, Yasmina; Karce, Houssam Eddine; Aggoun, Djouhra; Lanez, Touhami; Ruiz-Rosas, Ramiro; Bouzerafa, Brahim; Ourari, Ali; Morallon, Emilia

    2017-01-01

    This paper reports the synthesis, spectroscopic characterizations and electrochemical behavior of the obtained tetradentate copper (II)-Schiff base complex with its two wings as ferrocenylaniline moieties. This new ferrocenic derivative with two ferrocenylaniline entities surrounding the copper (II)-Salen complex (5) was synthesized by reacting N-ferrocenmethyl-N-phenyl-5-aminomethyl-2-hydroxyacetophenone (3) with one half equivalent of 1,2-diaminoethane in absolute ethanol. As for the interm...

  17. Model experiments on electrochemical formation of nano-dimensioned noble metal-oxide-semiconductor junctions at Si(1 1 1) surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Munoz, A.G., E-mail: andres.munoz@helmholtz-berlin.d [Institute for Solar Fuels and Energy Storage Materials, Helmholtz-Centre Berlin for Materials and Energy, Lise-Meitner Campus, Glienicker Strasse 100, D-14109 Berlin (Germany); Lewerenz, H.J. [Institute for Solar Fuels and Energy Storage Materials, Helmholtz-Centre Berlin for Materials and Energy, Lise-Meitner Campus, Glienicker Strasse 100, D-14109 Berlin (Germany)

    2010-11-01

    The recently introduced nanoemitter concept allows photovoltaic and photoelectrocatalytic energy conversion. Device functioning is presently based on metallic nanoemitters that are embedded in passivating films on Si absorbers. Model experiments on the electrodeposition of nanoscale noble metal islands onto n-type H:Si(1 1 1) are presented. Besides electrochemical methods such as impedance spectroscopy and cyclic voltammetry, atomic force microscopy (AFM), transmission electron microscopy (TEM) and synchrotron radiation photoelectron spectroscopy (SRPES) have been applied to elucidate the surface chemistry and electronics. The electrodeposition profiles of the reduction current under depletion condition indicate electron exchange via occupied surface states which strongly influence the deposition rate and the surface site selectivity of the nucleation process. SRPES at photon energies adjusted to high surface sensitivity shows formation of an ultrathin silicon dioxide film in the course of the reduction of the noble metal chloride complexes. The presence of this interfacial oxide is confirmed by high resolution TEM experiments. Step bunching at the Si surface upon electrodeposition is observed by AFM and analyzed in detail using (i) metal chloride complex containing solutions and (ii) chloride-ion solutions. A model for Si etching in chloride-ion containing solutions is presented that is also based on impedance measurements which show that Cl{sup -} is adsorbed at the Si surface. Finally, the successive steps of Pt electrodeposition from the hexachloro complex PtCl{sub 6}{sup 2-} onto Si(1 1 1) are outlined.

  18. A computation study on the interplay between surface morphology and electrochemical performance of patterned thin film electrodes for Li-ion batteries

    Science.gov (United States)

    Gur, Sourav; Frantziskonis, George N.; Aifantis, Katerina E.

    2017-08-01

    Recent experiments illustrate that the morphology of the electrode surface impacts the voltage - capacity curves and long term cycling performance of Li-ion batteries. The present study systematically explores the role of the electrode surface morphology and uncertainties in the reactions that occur during electrochemical cycling, by performing kinetic Monte Carlo (kMC) simulations using the lattice Boltzmann method (LBM). This allows encoding of the inherent stochasticity at discrete microscale reaction events over the deterministic mean field reaction dynamics that occur in Li-ion cells. The electrodes are taken to be dense thin films whose surfaces are patterned with conical, trapezoidal, dome-shaped, or pillar-shaped structures. It is shown that the inherent perturbations in the reactions together with the characteristics of the electrode surface configuration can significantly improve battery performance, mainly because patterned surfaces, as opposed to flat surfaces, result in a smaller voltage drop. The most efficient pattern was the trapezoidal, which is consistent with experimental evidence on Si patterned electrodes.

  19. High Power Electrochemical Capacitors

    Science.gov (United States)

    2012-03-23

    and Cu surfaces using trimethylamine alane (TMAA) as an organometallic CVD precursor. For this project we further demonstrated that the ALD deposition...this work, we show how the application of nanodiamond (ND) can greatly increase the performance of electrochemically active polymers , such as

  20. Working electrode holder and electrochemical cell

    DEFF Research Database (Denmark)

    2016-01-01

    The present disclosure relates to a holder for a test object, more specifically to a holder for measuring electrochemical properties of the test object. One embodiment relates to a working electrode holder for measuring electrochemical properties of a front surface of a test object in a liquid...... in the bottom surface and configured for passage of said liquid, such that liquid is able to pass onto the electrically contacted front surface. The holder may be used in an electrochemical cell....

  1. 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...

  2. Probing the Active Surface Sites for CO Reduction on Oxide-Derived Copper Electrocatalysts

    DEFF Research Database (Denmark)

    Verdaguer Casadevall, Arnau; Li, Christina W.; Johansson, Tobias Peter

    2015-01-01

    CO electroreduction activity on oxide-derived Cu (OD-Cu) was found to correlate with metastable surface features that bind CO strongly. OD-Cu electrodes prepared by H-2 reduction of Cu2O precursors reduce CO to acetate and ethanol with nearly 50% Faradaic efficiency at moderate overpotential. Tem...

  3. The derivation of scenic utility functions and surfaces and their role in landscape management

    Science.gov (United States)

    John W. Hamilton; Gregory J. Buhyoff; J. Douglas Wellman

    1979-01-01

    This paper outlines a methodological approach for determining relevant physical landscape features which people use in formulating judgments about scenic utility. This information, coupled with either empirically derived or rationally stipulated regression techniques, may be used to produce scenic utility functions and surfaces. These functions can provide a means for...

  4. Electrochemical Techniques

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Gang; Lin, Yuehe

    2008-07-20

    Sensitive and selective detection techniques are of crucial importance for capillary electrophoresis (CE), microfluidic chips, and other microfluidic systems. Electrochemical detectors have attracted considerable interest for microfluidic systems with features that include high sensitivity, inherent miniaturization of both the detection and control instrumentation, low cost and power demands, and high compatibility with microfabrication technology. The commonly used electrochemical detectors can be classified into three general modes: conductimetry, potentiometry, and amperometry.

  5. Aerosol optical depth under "clear" sky conditions derived from sea surface reflection of lidar signals.

    Science.gov (United States)

    He, Min; Hu, Yongxiang; Huang, Jian Ping; Stamnes, Knut

    2016-12-26

    There are considerable demands for accurate atmospheric correction of satellite observations of the sea surface or subsurface signal. Surface and sub-surface reflection under "clear" atmospheric conditions can be used to study atmospheric correction for the simplest possible situation. Here "clear" sky means a cloud-free atmosphere with sufficiently small aerosol particles. The "clear" aerosol concept is defined according to the spectral dependence of the scattering cross section on particle size. A 5-year combined CALIPSO and AMSR-E data set was used to derive the aerosol optical depth (AOD) from the lidar signal reflected from the sea surface. Compared with the traditional lidar-retrieved AOD, which relies on lidar backscattering measurements and an assumed lidar ratio, the AOD retrieved through the surface reflectance method depends on both scattering and absorption because it is based on two-way attenuation of the lidar signal transmitted to and then reflected from the surface. The results show that the clear sky AOD derived from the surface signal agrees with the clear sky AOD available in the CALIPSO level 2 database in the westerly wind belt located in the southern hemisphere, but yields significantly higher aerosol loadings in the tropics and in the northern hemisphere.

  6. Titanium Surface Coating with a Laminin-Derived Functional Peptide Promotes Bone Cell Adhesion

    Directory of Open Access Journals (Sweden)

    Seung-Ki Min

    2013-01-01

    Full Text Available Laminin-derived peptide coatings can enhance epithelial cell adhesion to implants, and the positive effect of these peptides on bone cell adhesion has been anticipated. The purpose of this study was to evaluate the improvement in bone cell attachment to and activity on titanium (Ti scaffolds coated with a laminin-derived functional peptide, Ln2-P3 (the DLTIDDSYWYRI motif. Four Ti disc surfaces were prepared, and a human osteosarcoma (HOS cell attachment test was performed to select two candidate surfaces for peptide coating. These two candidates were then coated with Ln2-P3 peptide, a scrambled peptide, or left uncoated to measure cell attachment to each surface, following which one surface was chosen to assess alkaline phosphatase (ALP activity and osteogenic marker gene expression with quantitative real-time PCR. On the commercially pure Ti surface, the Ln2-P3 coating significantly increased cellular ALP activity and the expression levels of ALP and bone sialoprotein mRNA as compared with the scrambled peptide-coated and uncoated surfaces. In conclusion, although further in vivo studies are needed, the findings of this in vitro study indicate that the Ln2-P3-coated implant surface promotes bone cell adhesion, which has clinical implications for reducing the overall treatment time of dental implant therapy.

  7. Synthesis of water-compatible surface-imprinted polymer via click chemistry and RAFT precipitation polymerization for highly selective and sensitive electrochemical assay of fenitrothion.

    Science.gov (United States)

    Zhao, Lijuan; Zhao, Faqiong; Zeng, Baizhao

    2014-12-15

    A novel water-compatible fenitrothion imprinted polymer was prepared on Au nanoparticles (AuNPs) by click chemistry and reversible addition-fragmentation chain transfer (RAFT) precipitation polymerization (RAFTPP). The RAFT chain-transfer agent was synthesized on the surface of AuNPs using click chemistry, then an imprinted polymer with hydrophilic polymer brushes was prepared on the RAFT chain-transfer agent modified AuNPs by RAFTPP, mediated by hydrophilic polyethylene glycol macromolecular cochain-transfer agent. The obtained molecularly imprinted material showed improved accessibility to fenitrothion and recognition property in water medium. When the material was immobilized on an ionic liquid functionalized graphene coated glassy carbon electrode for the electrochemical determination of fenitrothion, the resulting electrochemical sensor presented linear response in the range of 0.01-5 μM, with a sensitivity of 6.1 μA/μM mm(2). The low limit of detection was 8 nM (S/N=3). The sensor was successfully applied to the determination of real samples and the recovery for standard added was 95-108%. Copyright © 2014 Elsevier B.V. All rights reserved.

  8. An electrochemical impedimetric immunosensor for label-free detection of Campylobacter jejuni in diarrhea patients' stool based on O-carboxymethylchitosan surface modified Fe3O4 nanoparticles.

    Science.gov (United States)

    Huang, Jinlin; Yang, Gongjun; Meng, Wenjing; Wu, Liping; Zhu, Aiping; Jiao, Xin'an

    2010-01-15

    A novel electrochemical impedimetric immunosensor based on O-carboxymethylchitosan surface modified Fe(3)O(4) nanoparticles (denoted as OCMCS-Fe(3)O(4) nanoparticles) was developed for rapid detection of Campylobacter jejuni, which is becoming the most common cause of gastroenteritis in developed countries and raising major public health concerns worldwide. In the present study, anti-FlaA monoclonal antibodies 2D12 (denoted as 2D12McAbs) were immobilized on OCMCS-Fe(3)O(4) nanoparticles. The detection was performed by measuring relative change in impedance before and after 2D12McAbs-Campylobacter jejuni reaction with the technique of electrochemical impedance spectroscopy. Under the optimized conditions, the relative change in impedance was proportional to the logarithmic value of Campylobacter jejuni concentrations in the range of 1.0x10(3) to 1.0x10(7) CFU/mL (r=0.991). The advantages of the OCMCS-Fe(3)O(4) nanoparticle-based immunosensor are simplicity of use, fast response, wide linear range, acceptable reproducibility and long stability. Moreover, the immunosensor could be regenerated by being treated with glycine-HCl buffer solution (pH 2.8). We demonstrate the convenient application of the novel immunosensor for the detection of Campylobacter jejuni in diarrhea patients' stool samples. Copyright 2009 Elsevier B.V. All rights reserved.

  9. Electrochemical Surface Plasmon Resonance (EC-SPR) and Waveguide Enhanced Glucose Biosensing with N-Alkylaminated Polypyrrole/Glucose Oxidase Multilayers

    Science.gov (United States)

    Baba, Akira; Taranekar, Prasad; Ponnapati, Ramakrishna R.; Knoll, Wolfgang; Advincula, Rigoberto C.

    2010-01-01

    In this work, we report an electrochemical surface plasmon resonance/waveguide (EC-SPR/waveguide) glucose biosensor, which could detect enzymatic reactions in a conducting polymer/glucose oxidase (GOx) multilayer thin film. In order to achieve a controlled enzyme electrode and waveguide mode, GOx (negatively charged) was immobilized with a water-soluble conducting N-alkylaminated polypyrrole (positively charged) using the layer-by-layer (LbL) electrostatic self-assembly technique. The electrochemical and optical signals were simultaneously obtained from the composite LbL enzyme electrode upon addition of glucose as mediated by the electroactivity and electrochromic property of the polypyrrole layers. The signal enhancement in the EC-SPR detection is obtained by monitoring the doping-dedoping events on the polypyrrole. The real time optical signal could be distinguished between the change in the dielectric constant of the enzyme layer and other non-enzymatic reaction events such as adsorption of glucose and change of refractive index of solution. This was possible by a correlation of both the SPR mode, m=0, and m=1 mode of the waveguide in an SPR/waveguide spectroscopy experiment. PMID:20666478

  10. Signal reconstruction of surface waves on SASW measurement using Gaussian Derivative wavelet transform

    Science.gov (United States)

    Rosyidi, Sri; Taha, Mohd; Chik, Zamri; Ismail, Amiruddin

    2009-09-01

    Surface wave method consists of measurement and processing of the dispersive Rayleigh waves recorded from two or more vertical transducers. The dispersive phase data are inverted and the shear wave velocity versus depth is obtained. However, in case of residual soil, the reliable phase spectrum curve is difficult to be produced. Noises from nature and other human-made sources disturb the generated surface wave data. In this paper, a continuous wavelet transform based on mother wavelet of Gaussian Derivative was used to analyze seismic waves in different frequency and time. Time-frequency wavelet spectrum was employed to localize the interested seismic response spectrum of generated surface waves. It can also distinguish the fundamental mode of the surface wave from the higher modes of reflected body waves. The results presented in this paper showed that the wavelet analysis is able to determine reliable surface wave spectrum of sandy clayey residual soil.

  11. A data-derived forecast model of surface currents in a semi-enclosed bay (Yeosu Bay, Republic of Korea)

    Science.gov (United States)

    Won, S. I.; Kim, S. Y.

    2016-02-01

    We present a data-derived surface current forecast model based onobservations of high-frequency radar-derived surface currents, local winds, andalong-track altimeter-derived sea surface height anomalies off the southern coastof Korea (Yeosu Bay). The coastal surface circulation in this region is decomposedinto tide-, wind-, pressure gradient-coherent components depending on their forcingmechanisms in a hind cast model. The data-derived forecast model consistsof tidal harmonic analysis, response functions using wind stress and pressuregradients, and autoregressive process for residuals, These basis functions wereconsecutively added, and the performance of the forecast model is evaluated.

  12. Conductive surface modification of cauliflower-like WO{sub 3} and its electrochemical properties for lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Yoon, Sukeun, E-mail: skyoon@kongju.ac.kr [Division of Advanced Materials Engineering, Kongju National University, Chungnam 330-717 (Korea, Republic of); Woo, Sang-Gil [Advanced Batteries Research Center, Korea Electronics Technology Institute, Gyeonggi 463-816 (Korea, Republic of); Jung, Kyu-Nam [Energy Efficiency and Materials Research Division, Korea Institute of Energy Research, Daejeon 305-343 (Korea, Republic of); Song, Huesup, E-mail: hssong@kongju.ac.kr [Division of Advanced Materials Engineering, Kongju National University, Chungnam 330-717 (Korea, Republic of)

    2014-11-15

    Highlights: • Synthesis of cauliflower-like carbon-decorated WO{sub 3}. • Superior cyclability and rate capability for cauliflower-like carbon-decorated WO{sub 3}. • Electrochemical reaction behavior of cauliflower-like carbon-decorated WO{sub 3} with lithium. • In-situ XRD analysis during the first discharge–charge shows a complex reaction of intercalation and conversion of WO{sub 3}. - Abstract: Cauliflower-like WO{sub 3} was synthesized by a hydrothermal reaction without a surfactant, followed by firing, and was investigated as an anode material for lithium-ion battery applications. The scanning electron microscope (SEM) and transmission electron microscope (TEM) characterization indicated that WO{sub 3} nanorods had an aggregation framework and built a cauliflower morphology. With the objective of understanding the charge–discharge process within a voltage range of 0–3 V vs. Li{sup +}/Li, in situ X-ray diffraction was used and a complex reaction of intercalation and conversion of WO{sub 3} was revealed for the first time. The cauliflower-like WO{sub 3} after being decorated with carbon provides a high gravimetric capacity of >635 mA h/g (Li{sub 5.5}WO{sub 3}) with good cycling and a high rate capability when used as an anode in lithium-ion batteries. Based on our studies, we attribute the high electrochemical performance to the nanoscopic WO{sub 3} particles and a conductive carbon layer, which makes them a potential candidate for lithium-ion batteries.

  13. Electrochemical synthesis of nanostructured materials for electrochemical energy conversion and storage.

    Science.gov (United States)

    Li, Gao-Ren; Xu, Han; Lu, Xue-Feng; Feng, Jin-Xian; Tong, Ye-Xiang; Su, Cheng-Yong

    2013-05-21

    Electrochemical synthesis represents a highly efficient method for the fabrication of nanostructured energy materials, and various nanostructures, such as nanorods, nanowires, nanotubes, nanosheets, dendritic nanostructures, and composite nanostructures, can be easily fabricated with advantages of low cost, low synthetic temperature, high purity, simplicity, and environmental friendliness. The electrochemical synthesis, characterization, and application of electrochemical energy nanomaterials have advanced greatly in the past few decades, allowing an increasing understanding of nanostructure-property-performance relationships. Herein, we highlight some recent progress in the electrochemical synthesis of electrochemical energy materials with the assistance of additives and templates in solution or grafted onto metal or conductive polymer supports, with special attention to the effects on surface morphologies, structures and, more importantly, electrochemical performance. The methodology for preparing novel electrochemical energy nanomaterials and their potential applications has been summarized. Finally, we outline our personal perspectives on the electrochemical synthesis and applications of electrochemical energy nanomaterials.

  14. Improving evapotranspiration in a land surface model using biophysical variables derived from MSG/SEVIRI satellite

    Directory of Open Access Journals (Sweden)

    N. Ghilain

    2012-08-01

    Full Text Available Monitoring evapotranspiration over land is highly dependent on the surface state and vegetation dynamics. Data from spaceborn platforms are desirable to complement estimations from land surface models. The success of daily evapotranspiration monitoring at continental scale relies on the availability, quality and continuity of such data. The biophysical variables derived from SEVIRI on board the geostationary satellite Meteosat Second Generation (MSG and distributed by the Satellite Application Facility on Land surface Analysis (LSA-SAF are particularly interesting for such applications, as they aimed at providing continuous and consistent daily time series in near-real time over Africa, Europe and South America. In this paper, we compare them to monthly vegetation parameters from a database commonly used in numerical weather predictions (ECOCLIMAP-I, showing the benefits of the new daily products in detecting the spatial and temporal (seasonal and inter-annual variability of the vegetation, especially relevant over Africa. We propose a method to handle Leaf Area Index (LAI and Fractional Vegetation Cover (FVC products for evapotranspiration monitoring with a land surface model at 3–5 km spatial resolution. The method is conceived to be applicable for near-real time processes at continental scale and relies on the use of a land cover map. We assess the impact of using LSA-SAF biophysical variables compared to ECOCLIMAP-I on evapotranspiration estimated by the land surface model H-TESSEL. Comparison with in-situ observations in Europe and Africa shows an improved estimation of the evapotranspiration, especially in semi-arid climates. Finally, the impact on the land surface modelled evapotranspiration is compared over a north–south transect with a large gradient of vegetation and climate in Western Africa using LSA-SAF radiation forcing derived from remote sensing. Differences are highlighted. An evaluation against remote sensing derived land

  15. Lake Chad Total Surface Water Area as Derived from Land Surface Temperature and Radar Remote Sensing Data

    Directory of Open Access Journals (Sweden)

    Frederick Policelli

    2018-02-01

    Full Text Available Lake Chad, located in the middle of the African Sahel belt, underwent dramatic decreases in the 1970s and 1980s leaving less than ten percent of its 1960s surface water extent as open water. In this paper, we present an extended record (dry seasons 1988–2016 of the total surface water area of the lake (including both open water and flooded vegetation derived using Land Surface Temperature (LST data (dry seasons 2000–2016 from the NASA Terra MODIS sensor and EUMETSAT Meteosat-based LST measurements (dry seasons 1988–2001 from an earlier study. We also examine the total surface water area for Lake Chad using radar data (dry seasons 2015–2016 from the ESA Sentinel-1a mission. For the limited number of radar data sets available to us (18 data sets, we find on average a close match between the estimates from these data and the corresponding estimates from LST, though we find spatial differences in the estimates using the two types of data. We use these spatial differences to adjust the record (dry seasons 2000–2016 from MODIS LST. Then we use the adjusted record to remove the bias of the existing LST record (dry seasons 1988–2001 derived from Meteosat measurements and combine the two records. From this composite, extended record, we plot the total surface water area of the lake for the dry seasons of 1988–1989 through 2016–2017. We find for the dry seasons of 1988–1989 to 2016–2017 that the maximum total surface water area of the lake was approximately 16,800 sq. km (February and May, 2000, the minimum total surface water area of the lake was approximately 6400 sq. km (November, 1990, and the average was approximately 12,700 sq. km. Further, we find the total surface water area of the lake to be highly variable during this period, with an average rate of increase of approximately 143 km2 per year.

  16. Electrochemical Deposition of Zinc Oxide on the Surface of Composite Membrane Polysulfone-Graphene-Polystyrene in the Presence of Water Soluble Polymers

    Directory of Open Access Journals (Sweden)

    Alexandra Mocanu

    2017-01-01

    Full Text Available The aim of this study consisted in the development of an alternative synthesis procedure for hybrid ultrafiltration membranes for water purification. The membranes were obtained by wet-phase inversion method based on aliquots of polysulfone (PSF and graphene nanoplatelets modified with poly(styrene (G-PST. The hybrid materials were modified by electrochemical deposition of zinc oxide (ZnO on one side of the membranes in the presence of water soluble polymers. Raman, XPS, and TGA analyses were used to characterize the chemical and thermal characteristics of the PST-G. SEM analysis showed the formation of asymmetric porous configuration in all cases and the generation of ZnO with different shapes/structures on the bottom surface of the membrane or inside the porous channels. EDS analysis confirmed the formation of ZnO.

  17. How well Can We Classify SWOT-derived Water Surface Profiles?

    Science.gov (United States)

    Frasson, R. P. M.; Wei, R.; Picamilh, C.; Durand, M. T.

    2015-12-01

    The upcoming Surface Water Ocean Topography (SWOT) mission will detect water bodies and measure water surface elevation throughout the globe. Within its continental high resolution mask, SWOT is expected to deliver measurements of river width, water elevation and slope of rivers wider than ~50 m. The definition of river reaches is an integral step of the computation of discharge based on SWOT's observables. As poorly defined reaches can negatively affect the accuracy of discharge estimations, we seek strategies to break up rivers into physically meaningful sections. In the present work, we investigate how accurately we can classify water surface profiles based on simulated SWOT observations. We assume that most river sections can be classified as either M1 (mild slope, with depth larger than the normal depth), or A1 (adverse slope with depth larger than the critical depth). This assumption allows the classification to be based solely on the second derivative of water surface profiles, with convex profiles being classified as A1 and concave profiles as M1. We consider a HEC-RAS model of the Sacramento River as a representation of the true state of the river. We employ the SWOT instrument simulator to generate a synthetic pass of the river, which includes our best estimates of height measurement noise and geolocation errors. We process the resulting point cloud of water surface heights with the RiverObs package, which delineates the river center line and draws the water surface profile. Next, we identify inflection points in the water surface profile and classify the sections between the inflection points. Finally, we compare our limited classification of simulated SWOT-derived water surface profile to the "exact" classification of the modeled Sacramento River. With this exercise, we expect to determine if SWOT observations can be used to find inflection points in water surface profiles, which would bring knowledge of flow regimes into the definition of river reaches.

  18. Effect of Different Titanium Surfaces on Maturation of Murine Bone Marrow-Derived Dendritic Cells

    Science.gov (United States)

    Zheng, Xiaofei; Zhou, Fengjuan; Gu, Yifei; Duan, Xiaobo; Mo, Anchun

    2017-02-01

    Dendritic cells (DCs) play a pivotal role in the host response to implanted biomaterials. Osseointegration of titanium (Ti) implant is an immunological and inflammatory-driven process. However, the role of DCs in this complex process is largely unknown. This study aimed to investigate the effect of different Ti surfaces on DC maturation, and evaluate its subsequent potential on osteogenic differentiation of preosteoblasts. Murine bone marrow-derived DCs were seeded on Ti disks with different surface treatments, including pretreatment (PT), sandblasted/acid-etched (SLA) and modified SLA (modSLA) surface. Compared with DCs cultured on PT and SLA surfaces, the cells seeded on modSLA surface demonstrated a more round morphology with lower expression of CD86 and MHC-II, the DC maturation markers. Those cells also secreted high levels of anti-inflammatory cytokine IL-10 and TGF-β. Notably, addition of conditioned medium (CM) from modSLA-induced DCs significantly increased the mRNA expression of Runx2 and ALP as well as ALP activity by murine preosteoblast MC3T3-E1 cells. Our data demonstrated that Ti disks with different surfaces lead to differential DCs responses. PT and SLA surfaces induce DCs mature, while DCs seeded on modSLA-Ti surface maintain an immature phenotype and exhibit a potential of promoting osteogenic differentiation of MC3T3-E1 cells.

  19. Comparison of MODIS-derived land surface temperatures with ground surface and air temperature measurements in continuous permafrost terrain

    Directory of Open Access Journals (Sweden)

    S. Hachem

    2012-01-01

    Full Text Available Obtaining high resolution records of surface temperature from satellite sensors is important in the Arctic because meteorological stations are scarce and widely scattered in those vast and remote regions. Surface temperature is the primary climatic factor that governs the existence, spatial distribution and thermal regime of permafrost which is a major component of the terrestrial cryosphere. Land Surface (skin Temperatures (LST derived from the Moderate Resolution Imaging Spectroradiometer (MODIS sensor aboard the Terra and Aqua satellite platforms provide spatial estimates of near-surface temperature values. In this study, LST values from MODIS are compared to ground-based near-surface air (Tair and ground surface temperature (GST measurements obtained from 2000 to 2008 at herbaceous and shrub tundra sites located in the continuous permafrost zone of Northern Québec, Nunavik, Canada, and of the North Slope of Alaska, USA. LSTs (temperatures at the surface materials-atmosphere interface are found to be better correlated with Tair (1–3 m above the ground than with available GST (3–5 cm below the ground surface. As Tair is most often used by the permafrost community, this study focused on this parameter. LSTs are in stronger agreement with Tair during the snow cover season than in the snow free season. Combining Aqua and Terra LST-Day and LST-Nigh acquisitions into a mean daily value provides a large number of LST observations and a better overall agreement with Tair. Comparison between mean daily LSTs and mean daily Tair, for all sites and all seasons pooled together yields a very high correlation (R = 0.97; mean difference (MD = 1.8 °C; and standard deviation of MD (SD = 4.0 °C. The large SD can be explained by the influence of surface heterogeneity within the MODIS 1 km2 grid cells, the presence of undetected

  20. Modeling electrochemical resistance with coal surface properties in a direct carbon fuel cell based on molten carbonate

    Science.gov (United States)

    Eom, Seongyong; Ahn, Seongyool; Kang, Kijoong; Choi, Gyungmin

    2017-12-01

    In this study, a numerical model of activation and ohmic polarization is modified, taking into account the correlation function between surface properties and inner resistance. To investigate the correlation function, the surface properties of coal are changed by acid treatment, and the correlations between the inner resistance measured by half-cell tests and the surface characteristics are analyzed. A comparison between the model and experimental results demonstrates that the absolute average deviations for each fuel are less than 10%. The numerical results show that the sensitivities of the coal surface properties affecting polarization losses change depending on the operating temperature. The surface oxygen concentrations affect the activation polarization and the sensitivity decreased with increasing temperature. The surface ash of coal is an additional index to be considered along with ohmic polarization and it has the greatest effect on the surface properties at 973 K.

  1. Enhanced biofouling resistance of polyethersulfone membrane surface modified with capsaicin derivative and itaconic acid

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Jian [Key Laboratory of Marine Chemistry Theory and Technology, Ministry of Education, Ocean University of China, Qingdao 266100 (China); College of Chemistry and Chemical Engineering, Ocean University of China, Qingdao 266100 (China); Gao, Xueli, E-mail: gxl_ouc@126.com [Key Laboratory of Marine Chemistry Theory and Technology, Ministry of Education, Ocean University of China, Qingdao 266100 (China); College of Chemistry and Chemical Engineering, Ocean University of China, Qingdao 266100 (China); Wang, Qun; Sun, Haijing; Wang, Xiaojuan [Key Laboratory of Marine Chemistry Theory and Technology, Ministry of Education, Ocean University of China, Qingdao 266100 (China); College of Chemistry and Chemical Engineering, Ocean University of China, Qingdao 266100 (China); Gao, Congjie, E-mail: gaocjie@ouc.edu.cn [Key Laboratory of Marine Chemistry Theory and Technology, Ministry of Education, Ocean University of China, Qingdao 266100 (China); College of Chemistry and Chemical Engineering, Ocean University of China, Qingdao 266100 (China)

    2015-11-30

    Graphical abstract: - Highlights: • PES membrane was modified with a capsaicin derivative. • UV-assisted graft polymerization was carried out on membrane surface. • The capsaicin derivative modified membrane shows better antibiofouling property. - Abstract: The culprit of biofouling is the reproduction of viable microorganisms on the membrane surface. Recently, functionalization of membrane surface with natural antibacterial agents has drawn great attention. This work presents the fabrication of antibiofouling polyethersulfone (PES) ultrafiltration (UF) membranes by UV-assisted photo grafting of capsaicin derivative (N-(4-hydroxy-3-methoxy-benzyl)-acrylamide, HMBA) and itaconic acid (IA) on the surface of PES membrane. Results of FTIR-ATR, water static contact angle (WSCA) and atomic force microscopy (AFM) analysis confirmed the successful grafting of HMBA and IA on the membrane surface. We investigated the antifouling and antibacterial properties of these membranes using BSA and Escherichia coli as the test model, respectively. During a 150-min test, the modified membranes show much lower flux decline (42.7% for PES-g-1H0I, 22.2% for PES-g-1H1I and 7.7% for PES-g-1H5I) when compared with the pristine membrane (flux declined by 77%). The modified membranes exhibit excellent antibacterial activity (nearly 100%) when UV irradiation time was 6 min. The morphological study suggested that the E. coli on the pristine membrane showed a regular and smooth surface while that on the modified membrane was disrupted, which validated the antibacterial activity of the modified membranes.

  2. Mg-Fe-mixed oxides derived from layered double hydroxides: A study of the surface properties

    Directory of Open Access Journals (Sweden)

    Marinković-Nedučin Radmila P.

    2011-01-01

    Full Text Available The influence of surface properties on the selectivity of the synthesized catalysts was studied, considering that their selectivity towards particular hydrocarbons is crucial for their overall activity in the chosen Fischer- -Tropsch reaction. Magnesium- and iron-containing layered double hydroxides (LDH, with the general formula: [Mg1-xFex(OH2](CO3x/2?mH2O, x = = n(Fe/(n(Mg+n(Fe, synthesized with different Mg/Fe ratio and their thermally derived mixed oxides were investigated. Magnesium was chosen because of its basic properties, whereas iron was selected due to its well-known high Fischer-Tropsch activity, redox properties and the ability to form specific active sites in the layered LDH structure required for catalytic application. The thermally less stable multiphase system (synthesized outside the optimal single LDH phase range with additional Fe-phase, having a lower content of surface acid and base active sites, a lower surface area and smaller fraction of smaller mesopores, showed higher selectivity in the Fischer-Tropsch reaction. The results of this study imply that the metastability of derived multiphase oxides structure has a greater influence on the formation of specific catalyst surface sites than other investigated surface properties.

  3. Surfaces wettability and morphology modulation in a fluorene derivative self-assembly system

    Science.gov (United States)

    Cao, Xinhua; Gao, Aiping; Zhao, Na; Yuan, Fangyuan; Liu, Chenxi; Li, Ruru

    2016-04-01

    A new organogelator based on fluorene derivative (gelator 1) was designed and synthesized. Organogels could be obtained via the self-assembly of the derivative in acetone, toluene, ethyl acetate, hexane, DMSO and petroleum ether. The self-assembly process was thoroughly characterized using field-emission scanning electron microscopy (FESEM), X-ray diffraction (XRD), UV-vis, FT-IR and the contact angle. Surfaces with different morphologies and wetting properties were formed via the self-assembly of gelator 1 in the six different solvents. Interestingly, a superhydrophobic surface with a contact angle of 150° was obtained from organogel 1 in DMSO and exhibited the lotus-effect. The sliding angle necessary for a water droplet to move on the glass was only 15°. Hydrogen bonding and van der Waals forces were attributed as the main driving forces for gel formation.

  4. Interactions of Lysozyme and Azobenzene Derivatives in the Solution and on a Surface

    Science.gov (United States)

    Wei, Tao; Shing, Katherine

    2015-03-01

    The reversible isomerization of the azobenzene and its derivatives can control protein structure in an aqueous environment with the alternation of visible and UV lights for very promising applications in drug delivery. However, an atomistic description of Azo-molecules and protein amino acid residues is still lacking. In this study we performed atomistic molecular dynamics simulation to study the interactions between a lysozyme molecule and the Azobenzene derivative (in the bulk solution and grafted on the Silica surfaces). Protein structural arrangements (i.e., the shape and secondary structures) and its mobility, as a function of tran/cis ratio in the bulk solution and on the self-assembling monolayer surface's density and morphology, are systematically investigated.

  5. Utilization of kelp-derived carbon sources by kelp surface-associated bacteria

    OpenAIRE

    Bengtsson, Mia M.; Sjøtun, Kjersti; Storesund, Julia Endresen; Øvreås, Lise

    2011-01-01

    The surfaces of kelp are covered with bacteria that may utilize kelp-produced carbon and thereby contribute significantly to the carbon flux in kelp forest ecosystems. There is scant knowledge about the identity of these bacteria and about which kelp-derived carbon sources they utilize. An enrichment approach, using kelp constituent carbon sources for bacterial cultivation, was used to identify bacterial populations associated with the kelp Laminaria hyperborea that degrade kel...

  6. Guar gum as efficient non-toxic inhibitor of carbon steel corrosion in phosphoric acid medium: Electrochemical, surface, DFT and MD simulations studies

    Science.gov (United States)

    Messali, M.; Lgaz, H.; Dassanayake, R.; Salghi, R.; Jodeh, S.; Abidi, N.; Hamed, O.

    2017-10-01

    Guar gum is a water-soluble, nonionic, nontoxic, biodegradable and biocompatible hetero polysaccharide with unlimited number of industrial applications. In this study, guar gum was evaluated as a natural inhibitor of carbon steel (CS) corrosion in 2 M H3PO4 solution. The characteristic effect of guar gum on the steel corrosion was studied at concentration ranges from 0.1 to 1.0 g/L at 298-328 K by weight loss and electrochemical methods. Obtained results showed that, the inhibition efficiency (η%) of guar gum decreased slightly when the temperature increased and increased by increasing the inhibitor concentration reaching the maximum value at 1.0 g/L. The adsorption of guar gum on steel surface was studied by the Temkin adsorption model. EIS measurements indicate that the values of the polarization resistance (Rp) of CS in presence of guar gum are significantly higher than that of the untreated surface. Steel surface coated with guar gum was analyzed by SEM, FTIR and XRD. The quantum calculations using DFT method and Molecular Dynamic (MD) simulations were performed to define the relationship between inhibition performance of investigated compound and their molecular structure.

  7. Alkaloids extract of Retama monosperma (L.) Boiss. seeds used as novel eco-friendly inhibitor for carbon steel corrosion in 1 M HCl solution: Electrochemical and surface studies

    Science.gov (United States)

    El Hamdani, Naoual; Fdil, Rabiaa; Tourabi, Mustapha; Jama, Charafeddine; Bentiss, Fouad

    2015-12-01

    Current research efforts now focus on the development of non-toxic, inexpensive and environmentally friendly corrosion inhibitors as alternatives to different organic and non-organic compounds. In this field, alkaloids extract of Retama monosperma (L.) Boiss. seeds (AERS) was tested for the first time as corrosion inhibitor for carbon steel in 1 M HCl medium using electrochemical and surface characterization techniques. The obtained results showed that this plant extract's acts as an efficient corrosion inhibitor for carbon steel in 1 M HCl and an inhibition efficiency of 94.4% was reached with 400 mg/L of AERS at 30 °C. Ac impedance experimental data revealed a frequency distribution of the capacitance, simulated as constant phase element. Impedance results demonstrated that the addition of the AERS in the corrosive solution decreases the charge capacitance and simultaneously increases the function of the charge/discharge of the interface, facilitating the formation of an adsorbed layer over the steel surface. Polarization curves indicated that AERS is a mixed inhibitor. Adsorption of such alkaloid extract on the steel surface obeyed to the Langmuir adsorption isotherm. X-ray photoelectron spectroscopy (XPS) showed that the inhibition of steel corrosion in normal hydrochloric solution by AERS is mainly controlled by a physisorption process and the inhibitive layer is composed of an iron oxide/hydroxide mixture where AERS molecules are incorporated.

  8. Comparison of MODIS-derived land surface temperature with air temperature measurements

    Science.gov (United States)

    Georgiou, Andreas; Akçit, Nuhcan

    2017-09-01

    Air surface temperature is an important parameter for a wide range of applications such as agriculture, hydrology and climate change studies. Air temperature data is usually obtained from measurements made in meteorological stations, providing only limited information about spatial patterns over wide areas. The use of remote sensing data can help overcome this problem, particularly in areas with low station density, having the potential to improve the estimation of air surface temperature at both regional and global scales. Land Surface (skin) Temperatures (LST) derived from Moderate Resolution Imaging Spectroradiometer (MODIS) sensor aboard the Terra and Aqua satellite platforms provide spatial estimates of near-surface temperature values. In this study, LST values from MODIS are compared to groundbased near surface air (Tair) measurements obtained from 14 observational stations during 2011 to 2015, covering coastal, mountainous and urban areas over Cyprus. Combining Terra and Aqua LST-8 Day and Night acquisitions into a mean monthly value, provide a large number of LST observations and a better overall agreement with Tair. Comparison between mean monthly LSTs and mean monthly Tair for all sites and all seasons pooled together yields a very high correlation and biases. In addition, the presented high standard deviation can be explained by the influence of surface heterogeneity within MODIS 1km2 grid cells, the presence of undetected clouds and the inherent difference between LST and Tair. However, MODIS LST data proved to be a reliable proxy for surface temperature and mostly for studies requiring temperature reconstruction in areas with lack of observational stations.

  9. Electrochemically modified crystal orientation, surface morphology and optical properties using CTAB on Cu2O thin films

    Directory of Open Access Journals (Sweden)

    Karupanan Periyanan Ganesan

    Full Text Available Cuprous oxide (Cu2O thin films with different crystal orientations were electrochemically deposited in the presence of various molar concentrations of cetyl trimethyl ammonium bromide (CTAB on fluorine doped tin oxide (FTO glass substrate using standard three electrodes system. X-ray diffraction (XRD studies reveal cubic structure of Cu2O with (111 plane orientation, after addition of CTAB in deposition solution, the orientation of crystal changes from (111 into (200 plane. Scanning electron microscope (SEM images explored significant variation on morphology of Cu2O thin films deposited with addition of CTAB compared to without addition of CTAB. Photoluminescence (PL spectra illustrate that the emission peak around at 650 nm is attributed to near band edge emission, and the film prepared at the 3 mM of CTAB exhibits much higher intensity than that of the all other films. UV–Visible spectra show optical absorption in the range of 480–610 nm and the highest transparency of Cu2O film prepared at the concentration of 3 mM CTAB. The optical band gap is increased in the range between 2.16 and 2.45 eV with increasing the CTAB concentrations. Keywords: Cuprous oxide, Crystal orientation, Electrodeposition and cubic structure

  10. Oxidising alternative species to chromium VI in zinc-galvanised steel surface treatment. Part 2. An electrochemical study

    Energy Technology Data Exchange (ETDEWEB)

    Almeida, E. [Inst. Nacional de Engenharia e Tecnologia Industrial, Lisbon (Portugal); Fedrizzi, L. [Material Engineering Department, University of Trento, Trento (Italy); Diamantinio, T.C. [Inst. Nacional de Engenharia e Tecnologia Industrial, Lisbon (Portugal)]|[Instituto do Ambiente e Vida, Departamento de Zoologia, Universidade de Coimbra, Coimbra (Portugal)

    1998-06-05

    In the first part of this work, the authors present the main results and conclusions of a morphological and chemical study carried out on zinc conversion layers (ZCLs) obtained with oxidising alternative passivation baths, that includes molybdates, permanganates, vanadates and tungstates. A good chromate-based bath was used as reference. In this second part of the work, the authors present the main results obtained on selected zinc conversion layers (ZCLs), using a.c. electrochemical impedance spectroscopy (EIS). The results obtained were correlated with the morphological and chemical data obtained with the same ZCLs in the first part of this work. Finally, it is concluded that the alternative ZCLs studied, does not seem to be as efficient as that obtained with a chromate-based passivation bath used as reference. It is believed that a better understanding of the mechanisms involved in the ZCL`s formation, can be useful for studying, in the very near future, possible synergetic effects between molybdates and other chemical species. (orig.) 24 refs.

  11. Control of dental-derived induced pluripotent stem cells through modified surfaces for dental application.

    Science.gov (United States)

    Choi, Hyunmin; Park, Kyu-Hyung; Lee, Ah-Reum; Mun, Chin Hee; Shin, Yong Dae; Park, Yong-Beom; Park, Young-Bum

    2017-07-01

    The aim of this study is to investigate the behaviour of iPSc derived from dental stem cells in terms of initial adhesion, differentiation potential on differently surface-treated titanium disc. iPSc derived from human gingival fibroblasts (hGFs) were established using 4-reprogramming factors transduction with Sendai virus. The hGF-iPSc established in this study exhibited the morphology and growth properties similar to human embryonic stem (ES) cells and expressed pluripotency makers. Alkaline Phosphatase (AP) staining, Embryoid Body (EB) formation and in vitro differentiation and karyotyping further confirmed pluripotency of hGF-iPSc. Then, hGF-iPSc were cultured on machined- and Sandblasted and acid etched (SLA)-treated titanium discs with osteogenic induction medium and their morphological as well as quantitative changes according to different surface types were investigated using Alizrin Red S staining, Scanning electron microscopy (SEM), Flow cytometry and RT-PCR. Time-dependent and surface-dependent morphological changes as well as quantitative change in osteogenic differentiation of hGF-iPSc were identified and osteogenic gene expression of hGF-iPSc cultured on SLA-treated titanium disc found to be greater than machined titanium disc, suggesting the fate of hGF-iPSc may be determined by the characteristics of surface to which hGF-iPSc first adhere. iPSc derived from dental stem cell can be one of the most promising and practical cell sources for personalized regenerative dentistry and their morphological change as well as quantitative change in osteogenic differentiation according to different surface types may be further utilized for future clinical application incorporated with dental implant.

  12. Engineering the Surface/Interface Structures of Titanium Dioxide Micro and Nano Architectures towards Environmental and Electrochemical Applications

    DEFF Research Database (Denmark)

    Wang, Xiaoliang; Zhao, Yanyan; Mølhave, Kristian

    2017-01-01

    , with an emphasis on rational control of the surface and interface structures. We further discuss the applications of TiO₂ micro and nano architectures in photocatalysis, lithium/sodium ion batteries, and Li-S batteries. Throughout the discussion, the relationship between the device performance and the surface...

  13. Modified porous silicon for electrochemical sensor of para-nitrophenol

    Energy Technology Data Exchange (ETDEWEB)

    Belhousse, S., E-mail: all_samia_b@yahoo.fr [Centre de Recherche en Technologie des Semi-conducteurs pour l’Energétique (CRTSE), Division Thin Films-Surface and Interface, 2, Bd. Frantz Fanon, B.P. 140, Alger-7 merveilles, Algiers (Algeria); Belhaneche-Bensemra, N., E-mail: nbelhaneche@yahoo.fr [Ecole Nationale Polytechnique (ENP), 10, Avenue Hassen Badi, B.P. 182, 16200, El Harrach, Algiers (Algeria); Lasmi, K., E-mail: kahinalasmi@yahoo.fr [Centre de Recherche en Technologie des Semi-conducteurs pour l’Energétique (CRTSE), Division Thin Films-Surface and Interface, 2, Bd. Frantz Fanon, B.P. 140, Alger-7 merveilles, Algiers (Algeria); Mezaache, I., E-mail: lyeso_44@hotmail.fr [Ecole Nationale Polytechnique (ENP), 10, Avenue Hassen Badi, B.P. 182, 16200, El Harrach, Algiers (Algeria); Sedrati, T., E-mail: tarek_1990m@hotmail.fr [Ecole Nationale Polytechnique (ENP), 10, Avenue Hassen Badi, B.P. 182, 16200, El Harrach, Algiers (Algeria); Sam, S., E-mail: Sabrina.sam@polytechnique.edu [Centre de Recherche en Technologie des Semi-conducteurs pour l’Energétique (CRTSE), Division Thin Films-Surface and Interface, 2, Bd. Frantz Fanon, B.P. 140, Alger-7 merveilles, Algiers (Algeria); Tighilt, F.-Z., E-mail: mli_zola@yahoo.fr [Centre de Recherche en Technologie des Semi-conducteurs pour l’Energétique (CRTSE), Division Thin Films-Surface and Interface, 2, Bd. Frantz Fanon, B.P. 140, Alger-7 merveilles, Algiers (Algeria); Gabouze, N., E-mail: ngabouze@yahoo.fr [Centre de Recherche en Technologie des Semi-conducteurs pour l’Energétique (CRTSE), Division Thin Films-Surface and Interface, 2, Bd. Frantz Fanon, B.P. 140, Alger-7 merveilles, Algiers (Algeria)

    2014-11-15

    Highlights: • Hybrid device based on Porous silicon (PSi) and polythiophene (PTh) was prepared. • Three types of PSi/PTh hybrid structures were elaborated: PSi/PTh, oxide/PSi/PTh and Amino-propyltrimethoxysilane (APTMES)/oxide/PSi/PTh. • PTh was grafted on PSi using electrochemical polymerization. • The electrodetection of para-nitrophenol (p-NPh) was performed by cyclic voltammetry. • Oxide/PSi/PTh and APTMES/oxide/PSi/PTh, based electrochemical sensor showed a good response toward p-NPh. - Abstract: Hybrid structures based on polythiophene modified porous silicon was used for the electrochemical detection of para-nitrophenol, which is a toxic derivative of parathion insecticide and it is considered as a major toxic pollutant. The porous silicon was prepared by anodic etching in hydrofluodic acid. Polythiophene films were then grown by electropolymerisation of thiophene monomer on three different surfaces: hydrogenated PSi, oxidized PSi and amine-terminated PSi. The morphology of the obtained structures were observed by scanning electron microscopy and characterized by spectroscopy (FTIR). Cyclic voltammetry was used to study the electrochemical response of proposed structures to para-nitrophenol. The results show a high sensitivity of the sensor and a linearity of the electrochemical response in a large concentration interval ranging from 1.5 × 10{sup −8} M to the 3 × 10{sup −4}M.

  14. UV-assisted synthesis of surface modified mesoporous TiO{sub 2}/G microspheres and its electrochemical performances in lithium ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Tong, Xiaoling; Zeng, Min, E-mail: zengmin@swust.edu.cn; Li, Jing; Li, Fuyun

    2017-01-15

    Highlights: • We synthesize the surface modified mesoporous TiO{sub 2}/G microspheres, which possess high surface area with 258 m{sup 2} g{sup −1} and narrow pore size at about 7.8 nm. • The surface reaction mechanism of the UV-assisted synthesis mesoporous TiO{sub 2}/G microspheres has been explored. • The as-made TiO{sub 2}/G microspheres exhibit excellent electrochemical performances and deliver a capacity of 141 mAh g{sup −1} upon 100 cycles even at 1 C. - Abstract: Three-dimensional mesoporous TiO{sub 2}/graphene (TiO{sub 2}/G) microspheres have been successfully synthesized through a simple UV-assisted method of reduced graphene oxide with hydrazine. The as-made surface modified mesoporous TiO{sub 2}/G microspheres possess large surface area and exhibit a high initial discharge capacity of 220 mAh g{sup −1} and retain 84% (∼185 mAh g{sup −1}) of reversible capacity over 100 cycles at a rate of 0.2C. In addition, TiO{sub 2}/G microspheres display improved cyclic performance, excellent rate capability and enhanced electrical conductivity, which are superior to the bare TiO{sub 2} microspheres. Furthermore, TiO{sub 2}/G microspheres can achieve a reversible capacity of 141 mAh g{sup −1} upon 100 cycles even at the 1C rate. We believe that the mesoporous TiO{sub 2}/G microspheres are expected to be a promising high performance anode material for the next generation lithium ion batteries.

  15. 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....

  16. The Impact of Surface Chemistry on Bio-derived Carbon Performance as Supercapacitor Electrodes

    Science.gov (United States)

    Alshareef, Niman H.; Whitehair, Daniel; Xia, Chuan

    2017-03-01

    In this study, we demonstrate that highly functionalized and porous carbons can be derived from palm-leaf waste using the template-free facile synthesis process. The derived carbons have high content of nitrogen dopant, high surface area, and various defects. Moreover, these carbons exhibit a high electrical conductivity (107 S m-1). Thanks to the high content of edge N (64.3%) and highly microporous nature (82% of microspores), these biomass-derived carbons show promising performance when used as supercapacitor electrodes. To be specific, these carbonaceous materials show a specific capacitance as high as 197 and 135 F g-1 at 2 and 20 A g-1 in three-electrode configuration, respectively. Furthermore, the symmetrical cells using palm-leaf-derived carbon show an energy density of 8.4 Wh Kg-1 at a power density of 0.64 kW Kg-1, with high cycling life stability (˜8% loss after 10,000 continuous charge-discharge cycles at 20 A g-1). Interestingly, as the power density increases from 4.4 kW kg-1 to 36.8 kW kg-1, the energy density drops slowly from 8.4 Wh kg-1 to 3.4 Wh kg-1. Getting such extremely high power density without significant loss of energy density indicates that these palm-leaf-derived carbons have excellent electrode performance as supercapacitor electrodes.

  17. The Impact of Surface Chemistry on Bio-derived Carbon Performance as Supercapacitor Electrodes

    KAUST Repository

    Alshareef, Husam N.

    2016-12-23

    In this study, we demonstrate that highly functionalized and porous carbons can be derived from palm-leaf waste using the template-free facile synthesis process. The derived carbons have high content of nitrogen dopant, high surface area, and various defects. Moreover, these carbons exhibit a high electrical conductivity (107 S m−1). Thanks to the high content of edge N (64.3%) and highly microporous nature (82% of microspores), these biomass-derived carbons show promising performance when used as supercapacitor electrodes. To be specific, these carbonaceous materials show a specific capacitance as high as 197 and 135 F g−1 at 2 and 20 A g−1 in three-electrode configuration, respectively. Furthermore, the symmetrical cells using palm-leaf-derived carbon show an energy density of 8.4 Wh Kg−1 at a power density of 0.64 kW Kg−1, with high cycling life stability (∼8% loss after 10,000 continuous charge–discharge cycles at 20 A g−1). Interestingly, as the power density increases from 4.4 kW kg−1 to 36.8 kW kg−1, the energy density drops slowly from 8.4 Wh kg−1 to 3.4 Wh kg−1. Getting such extremely high power density without significant loss of energy density indicates that these palm-leaf-derived carbons have excellent electrode performance as supercapacitor electrodes.

  18. Modification of the cellulosic component of hemp fibers using sulfonic acid derivatives: Surface and thermal characterization.

    Science.gov (United States)

    George, Michael; Mussone, Paolo G; Bressler, David C

    2015-12-10

    The aim of this study was to characterize the surface, morphological, and thermal properties of hemp fibers treated with two commercially available, inexpensive, and water soluble sulfonic acid derivatives. Specifically, the cellulosic component of the fibers were targeted, because cellulose is not easily removed during chemical treatment. These acids have the potential to selectively transform the surfaces of natural fibers for composite applications. The proposed method proceeds in the absence of conventional organic solvents and high reaction temperatures. Surface chemical composition and signature were measured using gravimetric analysis, X-ray photoelectron spectroscopy (XPS) and Fourier transform infra-red spectroscopy (FTIR). XPS data from the treated hemp fibers were characterized by measuring the reduction in O/C ratio and an increase in abundance of the C-C-O signature. FTIR confirmed the reaction with the emergence of peaks characteristic of disubstituted benzene and amino groups. Grafting of the sulfonic derivatives resulted in lower surface polarity. Thermogravimetric analysis revealed that treated fibers were characterized by lower percent degradation between 200 and 300 °C, and a higher initial degradation temperature. Copyright © 2015 Elsevier Ltd. All rights reserved.

  19. Three-dimensional surface deformation derived from airborne interferometric UAVSAR: Application to the Slumgullion Landslide

    Science.gov (United States)

    Delbridge, Brent G.; Bürgmann, Roland; Fielding, Eric; Hensley, Scott; Schulz, William H.

    2016-05-01

    In order to provide surface geodetic measurements with "landslide-wide" spatial coverage, we develop and validate a method for the characterization of 3-D surface deformation using the unique capabilities of the Uninhabited Aerial Vehicle Synthetic Aperture Radar (UAVSAR) airborne repeat-pass radar interferometry system. We apply our method at the well-studied Slumgullion Landslide, which is 3.9 km long and moves persistently at rates up to ˜2 cm/day. A comparison with concurrent GPS measurements validates this method and shows that it provides reliable and accurate 3-D surface deformation measurements. The UAVSAR-derived vector velocity field measurements accurately capture the sharp boundaries defining previously identified kinematic units and geomorphic domains within the landslide. We acquired data across the landslide during spring and summer and identify that the landslide moves more slowly during summer except at its head, presumably in response to spatiotemporal variations in snowmelt infiltration. In order to constrain the mechanics controlling landslide motion from surface velocity measurements, we present an inversion framework for the extraction of slide thickness and basal geometry from dense 3-D surface velocity fields. We find that the average depth of the Slumgullion Landslide is 7.5 m, several meters less than previous depth estimates. We show that by considering a viscoplastic rheology, we can derive tighter theoretical bounds on the rheological parameter relating mean horizontal flow rate to surface velocity. Using inclinometer data for slow-moving, clay-rich landslides across the globe, we find a consistent value for the rheological parameter of 0.85 ± 0.08.

  20. Impact Of Strain In Drawing Process And Surface Modification On Resistance To Electrochemical Corrosion Of Wires Used In Dentistry

    National Research Council Canada - National Science Library

    J. Przondziono; E. Hadasik; W. Walke; J. Szala

    2015-01-01

    The study presents the results of research into the impact of strain in cold drawing and surface modification treatment on corrosion properties of wires made of X10CrNi 18-8 steel used in maxillofacial surgery...

  1. Solution Process Synthesis of High Aspect Ratio ZnO Nanorods on Electrode Surface for Sensitive Electrochemical Detection of Uric Acid

    Science.gov (United States)

    Ahmad, Rafiq; Tripathy, Nirmalya; Ahn, Min-Sang; Hahn, Yoon-Bong

    2017-04-01

    This study demonstrates a highly stable, selective and sensitive uric acid (UA) biosensor based on high aspect ratio zinc oxide nanorods (ZNRs) vertical grown on electrode surface via a simple one-step low temperature solution route. Uricase enzyme was immobilized on the ZNRs followed by Nafion covering to fabricate UA sensing electrodes (Nafion/Uricase-ZNRs/Ag). The fabricated electrodes showed enhanced performance with attractive analytical response, such as a high sensitivity of 239.67 μA cm-2 mM-1 in wide-linear range (0.01-4.56 mM), rapid response time (~3 s), low detection limit (5 nM), and low value of apparent Michaelis-Menten constant (Kmapp, 0.025 mM). In addition, selectivity, reproducibility and long-term storage stability of biosensor was also demonstrated. These results can be attributed to the high aspect ratio of vertically grown ZNRs which provides high surface area leading to enhanced enzyme immobilization, high electrocatalytic activity, and direct electron transfer during electrochemical detection of UA. We expect that this biosensor platform will be advantageous to fabricate ultrasensitive, robust, low-cost sensing device for numerous analyte detection.

  2. Surface diurnal warming in the East China Sea derived from satellite remote sensing

    Science.gov (United States)

    Song, Dan; Duan, Zhigang; Zhai, Fangguo; He, Qiqi

    2017-09-01

    Process of sea surface diurnal warming has drawn a lot of attention in recent years, but that occurs in shelf seas was rarely addressed. In the present work, surface diurnal warming strength in the East China Sea was calculated by the sea surface temperature (SST) data derived from the MODIS sensors carried by the satellites Aqua and Terra. Due to transit time difference, both the number of valid data and the surface diurnal warming strength computed by the MODIS-Aqua data are relatively larger than Terra. Therefore, the 10-year MODIS-Aqua data from 2005 to 2014 were used to analyze the monthly variability of the surface diurnal warming. Generally, the surface diurnal warming in the East China sea is stronger in summer and autumn but weaker in winter and spring, while it shows different peaks in different regions. Large events with ΔT≥5 K have also been discussed. They were found mainly in coastal area, especially near the Changjiang (Yangtze) River estuary. And there exists a high-incidence period from April to July. Furthermore, the relationship between surface diurnal warming and wind speed was discussed. Larger diurnal warming mainly lies in areas with low wind speed. And its possibility decreases with the increase of wind speed. Events with ΔT≥2.5 K rarely occur when wind speed is over 12 m/s. Study on surface diurnal warming in the East China Sea may help to understand the daily scale air-sea interaction in the shelf seas. A potential application might be in the marine weather forecasts by numerical models. Its impact on the coastal eco-system and the activities of marine organisms can also be pursued.

  3. XPS and electrochemical impedance spectroscopy studies on effects of the porcelain firing process on surface and corrosion properties of two nickel-chromium dental alloys.

    Science.gov (United States)

    Qiu, Jing; Tang, Chun-bo; Zhu, Zhi-jun; Zhou, Guo-xing; Wang, Jie; Yang, Yi; Wang, Guo-ping

    2013-11-01

    The aim of this study was to evaluate the effects of a simulated porcelain firing process on the surface, corrosion behavior and cell culture response of two nickel-chromium (Ni-Cr) dental alloys. A Be-free alloy and a Be-containing alloy were tested. Before porcelain firing, as-cast specimens were examined for surface composition using X-ray photoelectron spectroscopy and metallurgical phases using X-ray diffraction. Corrosion behaviors were evaluated using electrochemical impedance spectroscopy. 3T3 fibroblasts were cultured and exposed indirectly to specimens. MTT assays were counted after 3 and 6 days. The cell culture mediums exposed to specimens were analyzed for metal ion release. After porcelain firing, similar specimens were examined for the same properties. In both as-cast and fired conditions, the Be-free Ni-Cr alloy showed significantly more resistance to corrosion than the Be-containing Ni-Cr alloy, which exhibited BeNi phase. After porcelain firing, the corrosion resistance of the Be-free Ni-Cr alloy decreased statistically, corresponding with evident decreases of Cr and Ni oxides on the alloy surface. Also, the alloy's MTT assay decreased significantly corresponding with an obvious increase of Ni-ion release after the firing. For the Be-containing Ni-Cr alloy, the firing process led to increases of surface oxides and metallic Be, while its corrosion resistance and cell culture response were not significantly changed after porcelain firing. The results suggested that the corrosion resistance and biocompatibility of the Be-free Ni-Cr alloy decreased after porcelain firing, whereas the firing process had little effect on the same properties of the Be-containing Ni-Cr alloy.

  4. Alkaloids extract of Retama monosperma (L.) Boiss. seeds used as novel eco-friendly inhibitor for carbon steel corrosion in 1 M HCl solution: Electrochemical and surface studies

    Energy Technology Data Exchange (ETDEWEB)

    El Hamdani, Naoual; Fdil, Rabiaa [Laboratoire de Chimie Bioorganique, Faculté des Sciences, Université Chouaib Doukkali, B.P. 20, M-24000 El Jadida (Morocco); Tourabi, Mustapha [Laboratoire de Catalyse et de Corrosion des Matériaux (LCCM), Faculté des Sciences, Université Chouaib Doukkali, B.P. 20, M-24000 El Jadida (Morocco); Jama, Charafeddine [UMET-PSI, CNRS UMR 8207, ENSCL, Université Lille 1, CS 90108, F-59652 Villeneuve d’Ascq Cedex (France); Bentiss, Fouad, E-mail: fbentiss@enscl.fr [Laboratoire de Catalyse et de Corrosion des Matériaux (LCCM), Faculté des Sciences, Université Chouaib Doukkali, B.P. 20, M-24000 El Jadida (Morocco); UMET-PSI, CNRS UMR 8207, ENSCL, Université Lille 1, CS 90108, F-59652 Villeneuve d’Ascq Cedex (France)

    2015-12-01

    Graphical abstract: - Highlights: • AERS is good eco-friendly corrosion inhibitor for carbon steel in 1 M HCl. • AERS acts as mixed-type inhibitor in 1 M HCl medium. • AERS adsorption is well described by Langmuir isotherm. • Surface analyses were used to explain the AERS mechanism of carbon steel corrosion inhibition. - Abstract: Current research efforts now focus on the development of non-toxic, inexpensive and environmentally friendly corrosion inhibitors as alternatives to different organic and non-organic compounds. In this field, alkaloids extract of Retama monosperma (L.) Boiss. seeds (AERS) was tested for the first time as corrosion inhibitor for carbon steel in 1 M HCl medium using electrochemical and surface characterization techniques. The obtained results showed that this plant extract's acts as an efficient corrosion inhibitor for carbon steel in 1 M HCl and an inhibition efficiency of 94.4% was reached with 400 mg/L of AERS at 30 °C. Ac impedance experimental data revealed a frequency distribution of the capacitance, simulated as constant phase element. Impedance results demonstrated that the addition of the AERS in the corrosive solution decreases the charge capacitance and simultaneously increases the function of the charge/discharge of the interface, facilitating the formation of an adsorbed layer over the steel surface. Polarization curves indicated that AERS is a mixed inhibitor. Adsorption of such alkaloid extract on the steel surface obeyed to the Langmuir adsorption isotherm. X-ray photoelectron spectroscopy (XPS) showed that the inhibition of steel corrosion in normal hydrochloric solution by AERS is mainly controlled by a physisorption process and the inhibitive layer is composed of an iron oxide/hydroxide mixture where AERS molecules are incorporated.

  5. Electrochemical functionalization of vertically aligned carbon nanotube arrays with molybdenum oxides for the development of a surface-charge-controlled sensor

    Energy Technology Data Exchange (ETDEWEB)

    Ye, J-S [Department of Biological Sciences, National University of Singapore, 14 Science Drive 4, 117543, Singapore (Singapore); Wen Ying [Department of Chemistry, National University of Singapore, 3 Science Drive 3, 117543, Singapore (Singapore); Zhang, W-D [Nano Science Research Center, College of Chemistry, South China University of Technology, Guangzhou 510640 (China); Cui, H F [Department of Biological Sciences, National University of Singapore, 14 Science Drive 4, 117543, Singapore (Singapore); Xu, G Q [Department of Chemistry, National University of Singapore, 3 Science Drive 3, 117543, Singapore (Singapore); Sheu, F-S [Department of Biological Sciences, National University of Singapore, 14 Science Drive 4, 117543, Singapore (Singapore)

    2006-08-14

    The modification of inorganic polymeric oxides at the surface of carbon nanotubes is of paramount importance for developing new sensors. In this study, molybdenum oxide (MoO{sub x}) film was electrodeposited on the surface of multi-walled carbon nanotubes (MWNTs) by cycling the potential between +0.20 and -0.80 V (versus 3 M KCl-Ag|AgCl) in Na{sub 2}MoO{sub 4} solution. The MoO{sub x}-modified nanotube (MoO{sub x}/MWNT) electrode displays well-defined redox transitions in 5 mM H{sub 2}SO{sub 4} or in phosphate buffer solution (PBS), which can be attributed to the reductive formation and the re-oxidation of hydrogen molybdenum oxides. X-ray photoelectron spectra (XPS) showed that the deposited MoO{sub x} films are mainly Mo{sup 6+} complexes. Both MWNT and MoO{sub x}/MWNT electrodes have ideal reversibility in 5 mM K{sub 3}[Fe(CN){sub 6}] in 1 M KCl as supporting electrolytes at all sweep rates (0.02-1.00 V s{sup -1}) by cyclic voltammetry. The negatively charged surface of MoO{sub x}/MWNTs can further attract molecular cations such as Ru(NH{sub 3}){sub 6}{sup 3+}. The MoO{sub x}/MWNT electrode exhibited electrocatalytic ability towards the reduction of bromate due to high surface area and the fast electron transfer rate of nanotubes. Thus, electrochemical modification of inorganic polymeric oxides on the carbon nanotube provides a simple method for the preparation of novel sensors.

  6. Electrochemical nanomoulding through proteins

    Science.gov (United States)

    Allred, Daniel B.

    The continued improvements in performance of modern electronic devices are directly related to the manufacturing of smaller, denser features on surfaces. Electrochemical fabrication has played a large role in continuing this trend due to its low cost and ease of scaleability toward ever smaller dimensions. This work introduces the concept of using proteins, essentially monodisperse complex polymers whose three-dimensional structures are fixed by their encoded amino acid sequences, as "moulds" around which nanostructures can be built by electrochemical fabrication. Bacterial cell-surface layer proteins, or "S-layer" proteins, from two organisms---Deinococcus radiodurans and Sporosarcina ureae---were used as the "moulds" for electrochemical fabrication. The proteins are easily purified as micron-sized sheets of periodic molecular complexes with 18-nm hexagonal and 13-nm square unit cell lattices, respectively. Direct imaging by transmission electron microscopy on ultrathin noble metal films without sample preparation eliminates potential artifacts to the high surface energy substrates necessary for high nucleation densities. Characterization involved imaging, electron diffraction, spectroscopy, and three-dimensional reconstruction. The S-layer protein of D. radiodurans was further subjected to an atomic force microscope based assay to determine the integrity of its structure and long-range order and was found to be useful for fabrication from around pH 3 to 12.

  7. Surface markers of heterogeneous peripheral blood-derived smooth muscle progenitor cells.

    Science.gov (United States)

    Wang, Chao-Hung; Lee, Yun-Shien; Lin, Shing-Jong; Mei, Hsiu-Fu; Lin, Sheng-Yuan; Liu, Min-Hui; Chen, Jim-Ray; Cherng, Wen-Jin

    2012-08-01

    Smooth muscle progenitor cells (SMPCs) were intriguingly shown to act as a double-edged sword in the pathogenesis of atherosclerosis. To fully clarify the roles of SMPCs in atherosclerosis, a distinct panel of SMPC surface markers is mandatory to be developed. Microarray gene expression analyses were used to discover potential surface markers of SMPCs. In vitro and in vivo experiments documented that platelet-derived growth factor receptor-β, carboxypeptidase M, carbonic anhydrase 12, receptor activity-modifying protein 1, and low-density lipoprotein receptor-related protein were the 5 specific surface markers regulating various SMPC functions, including migration, extracellular matrix formation, resistance to hypoxia, and anti-inflammation. In severe combined immunodeficiency/nonobese diabetic mice after femoral arterial wire injury, injected human peripheral blood mononuclear cells contributed to substantial amount of neointimal α-smooth muscle actin-positive cells, coexpressing platelet-derived growth factor receptor-β, carboxypeptidase M, carbonic anhydrase 12, receptor activity-modifying protein 1, and low-density lipoprotein receptor-related protein. Based on these markers, a novel quantification assay was developed to enumerate circulating early SMPC. Early SMPC numbers were higher in patients with unstable angina compared with those with normal coronary angiograms. In patients with acute ST-elevation myocardial infarction, different patterns of serial early SMPC changes were noted, related to different clinical presentations. Surface markers of heterogeneous SMPCs exhibit various functions associated with atherosclerotic pathophysiology. Quantification of surface marker-defined SMPCs provides a platform for studying SMPCs in cardiovascular diseases.

  8. The higher mode of surface wave derived from ambient noise and preliminary application to estimating subsurface

    Science.gov (United States)

    Zhentao, Y.; Xiaofei, C.; Jiannan, W.

    2016-12-01

    The fundamental mode is the primary component of surface wave derived from ambient noise. It is the basis of the method of structure imaging from ambient noise (e.g. SPAC, Aki 1957; F-K, Lascoss 1968; MUSIC, Schmidt 1986). It is well known, however, that if the higher modes of surface wave can be identified from data and are incorporated in the inversion of dispersion curves, the uncertainty in inversion results will be greatly reduced (e.g., Tokimastu,1997). Actually, the ambient noise indeed contains the higher modes as well in its raw data of ambient noise. If we could extract the higher modes from ambient noise, the structure inversion method of ambient noise would be greatly improved. In the past decade, there are many studies to improve SPAC and analyses the relationship of fundamental mode and higher mode (Ohri et al 2002; Asten et al. 2006; Tashiaki Ykoi 2010 ;Tatsunori Ikeda 2012). In this study, we will present a new method of identifying higher modes from ambient noise data by reprocessing the "surface waves' phases" derived from the ambient noise through cross-correlation analysis, and show preliminary application in structure inversion.

  9. Surfaces wettability and morphology modulation in a fluorene derivative self-assembly system

    Energy Technology Data Exchange (ETDEWEB)

    Cao, Xinhua, E-mail: caoxhchem@163.com; Gao, Aiping; Zhao, Na; Yuan, Fangyuan; Liu, Chenxi; Li, Ruru

    2016-04-15

    Graphical abstract: - Highlights: • The different structures could be obtained in this self-assembly system. • A water-drop could freely roll on the xerogel film with the sliding angle of 15.0. • The superhydrophobic surface can be obtained via supramolecular self-assembly. - Abstract: A new organogelator based on fluorene derivative (gelator 1) was designed and synthesized. Organogels could be obtained via the self-assembly of the derivative in acetone, toluene, ethyl acetate, hexane, DMSO and petroleum ether. The self-assembly process was thoroughly characterized using field-emission scanning electron microscopy (FESEM), X-ray diffraction (XRD), UV–vis, FT-IR and the contact angle. Surfaces with different morphologies and wetting properties were formed via the self-assembly of gelator 1 in the six different solvents. Interestingly, a superhydrophobic surface with a contact angle of 150° was obtained from organogel 1 in DMSO and exhibited the lotus-effect. The sliding angle necessary for a water droplet to move on the glass was only 15°. Hydrogen bonding and van der Waals forces were attributed as the main driving forces for gel formation.

  10. Hydrophilic monolayer formation of adsorbed cationic starch and cationic hydroxyethyl cellulose derivatives on polyester surfaces.

    Science.gov (United States)

    Roos, Peter; Westling, Asa; Chronakis, Ioannis S

    2004-11-01

    Cationic starch, cationic cellulose derivatives, and hydrophobically modified cationic cellulose were physically adsorbed from aqueous solution onto oppositely charged hydrophobic polyester (poly(ethylene terephthalate)) fabric and nonwoven, and this resulted in hydrophilic surface properties. Surface coverage of the polysaccharides occurred primarily by strong electrostatic interactions, and the surface characteristics were evaluated by measuring the time required for a water droplet to be absorbed into the polyester material as well as by electron spectroscopy for chemical analysis (ESCA). From a comparison of the adsorption characteristics we assess the polysaccharide-dependent and substrate-dependent adsorption behavior and discuss the similarities and differences in the hydrophilic properties and wettability observed. In particular, the temperature of the cationic polysaccharide solutions in which the substrate was immersed, the configuration of the polymer in solution, and the presence of hydrophobic substituents on the cationic moiety have a considerable effect on the polysaccharide affinity and its adsorption on the surface, irrespective of the substrate type (fabric or nonwoven). We also evaluate the relative contribution of the polyelectrolyte molecular weight, concentration in solution, and degree of charge density along the polymer chain which determine the range of interactions and alter surface hydroplilicity dependent on the type of substrate.

  11. Adsorption of cationic hydroxyethylcellulose derivatives onto planar and curved gold surfaces.

    Science.gov (United States)

    Pamies, Ramón; Volden, Sondre; Kjøniksen, Anna-Lena; Zhu, Kaizheng; Glomm, Wilhelm R; Nyström, Bo

    2010-10-19

    The adsorption of two positively charged hydroxyethylcellulose derivatives with 7 and 60 mol % positively charged groups and a cationic, hydrophobically modified hydroxyethylcellulose containing 1 mol % hydrophobic groups and 7 mol % charged groups onto flat and spherical citrate-coated gold surfaces of different sizes has been investigated. The planar surfaces were studied by means of the quartz crystal microbalance with dissipation monitoring, whereas nanoparticle suspensions were examined using dynamic light scattering and UV-vis spectroscopy. Two different driving forces for adsorption have been evaluated: the electrostatic interaction between the positive charges on the polymers and the negatively charged gold surfaces and the affinity of the polymers for gold due to hydrophobic interactions. The comparison between the data obtained from curved and planar surfaces suggests a strong correlation between surface curvature and adlayer conformation in the formation of the hybrid polymer-gold nanoparticles. The influence of particle size on the amount of adsorbed polymer has been evaluated for the different polymers. The impact of the ionic strength on polymer adsorption has been explored, and the adsorbed polymer layer has been found to protect the gold nanoparticles from aggregation when salt is added to the solution. The addition of salt to a mixture of gold particles and a charged polymer can induce a thicker adsorbed layer at low salinity, and desorption was found at high levels of salt addition.

  12. Use of cellulose derivatives on gold surfaces for reduced nonspecific adsorption of immunoglobulin G.

    Science.gov (United States)

    Volden, Sondre; Zhu, Kaizheng; Nyström, Bo; Glomm, Wilhelm R

    2009-09-01

    This study addresses the design of protein-repellent gold surfaces using hydroxyethyl- and ethyl(hydroxyethyl) cellulose (HEC and EHEC) and hydrophobically modified analogues of these polymers (HM-HEC and HM-EHEC). Adsorption behavior of the protein immunoglobulin G (IgG) onto pure gold and gold surfaces coated with cellulose polymers was investigated and described by quartz crystal microbalance with dissipation monitoring (QCM-D), atomic force microscopy (AFM) and contact angle measurements (CAM). Surfaces coated with the hydrophobically modified cellulose derivatives were found to significantly outperform a reference poly(ethylene glycol) (PEG) coating, which in turn prevented 90% of non-specific protein adsorption as compared to adsorption onto pure gold. HEC and EHEC prevented around 30% and 60% of the IgG adsorption observed on pure gold, while HM-HEC and HM-EHEC were both found to completely hinder biofouling when deposited on the gold substrates. Adsorption behavior of IgG has been discussed in terms of polymer surface coverage and roughness of the applied surfaces, together with hydrophobic interactions between protein and gold, and also polymer-protein interactions.

  13. Electrochemical CO2 reduction on Au surfaces: mechanistic aspects regarding the formation of major and minor products.

    Science.gov (United States)

    Cave, Etosha R; Montoya, Joseph H; Kuhl, Kendra P; Abram, David N; Hatsukade, Toru; Shi, Chuan; Hahn, Christopher; Nørskov, Jens K; Jaramillo, Thomas F

    2017-06-21

    In the future, industrial CO2 electroreduction using renewable energy sources could be a sustainable means to convert CO2 and water into commodity chemicals at room temperature and atmospheric pressure. This study focuses on the electrocatalytic reduction of CO2 on polycrystalline Au surfaces, which have high activity and selectivity for CO evolution. We explore the catalytic behavior of polycrystalline Au surfaces by coupling potentiostatic CO2 electrolysis experiments in an aqueous bicarbonate solution with high sensitivity product detection methods. We observed the production of methanol, in addition to detecting the known products of CO2 electroreduction on Au: CO, H2 and formate. We suggest a mechanism that explains Au's evolution of methanol. Specifically, the Au surface does not favor C-O scission, and thus is more selective towards methanol than methane. These insights could aid in the design of electrocatalysts that are selective for CO2 electroreduction to oxygenates over hydrocarbons.

  14. Estimation of Sway Velocity-Dependent Hydrodynamic Derivatives in Surface Ship Manoeuvring Using Ranse Based CFD

    Directory of Open Access Journals (Sweden)

    Sheeja Janardhanan

    2010-09-01

    Full Text Available The hydrodynamic derivatives appearing in the manoeuvring equations of motion are the primary parameters in the prediction of the trajectory of a vessel. Determination of these derivatives poses major challenge in ship manoeuvring related problems. This paper deals with one such problem in which an attempt has been made to numerically simulate the conventional straight line test in a towing tank using computational fluid dynamics (CFD. Free-surface effects have been neglected here. The domain size has been fixed as per ITTC guide lines. The grid size has been fixed after a thorough grid independency analysis and an optimum grid size has been chosen in order to ensure the insensitivity of the flow parameters to grid size and also to have reduced computational effort. The model has been oriented to wider range of drift angles to capture the non-linear effects and subsequently the forces and moments acting on the model in each angle have been estimated. The sway velocity dependent derivatives have been obtained through plots and curve-fits. The effect of finite water depth on the derivatives has also been looked into. The results have been compared with the available experimental and empirical values and the method was found to be promising.

  15. Microscopically derived potential-energy surfaces for the chain of Sm-isotopes

    Energy Technology Data Exchange (ETDEWEB)

    Van Geel, H. (Institut fuer Theoretische Physik, J.W. v. Goethe-Universitaet, Robert-Mayer-Str. 8-10, D-60054 Frankfurt am Main (Germany)); Hess, P.O. (Institut fuer Theoretische Physik, Justus-Liebig-Universitaet, Heinrich-Buff-Ring 16, D-35392 Giessen (Germany)); Troltenier, D. (Institut fuer Theoretische Physik, J.W. v. Goethe-Universitaet, Robert-Mayer-Str. 8-10, D-60054 Frankfurt am Main (Germany)); Maruhn, J.A. (Joint Institute for Heavy Ion Research, Holifield Heavy Ion Research Facility, Oak Ridge, TN 37831 (United States)); Greiner, W. (Joint Institute for Heavy Ion Research, Holifield Heavy Ion Research Facility, Oak Ridge, TN 37831 (United States) Department of Physics and Astronomy, Vanderbilt University, Nashville, TN 37235 (United States))

    1994-09-26

    An extended method is presented to microscopically derive potential energy surfaces (PES) for quadrupole-deformed nuclei. The underlying microscopic theory is a symplectic model. Coherent states play a dominant role in the derivation and the Nilsson orbitals are used to extract level occupations. Taking into account the rearrangement in the occupation due to variations in the deformation and the resulting relative change in the zero-point energy, we obtain PESs for [sup 148]Sm, [sup 150]Sm and [sup 152]Sm without resorting to a fit to experimental data. The mass parameter is fitted to the first 6[sup +] state, applying a calculation within the phenomenological geometric model. We achieve good qualitative agreement with the experiments. As special features we obtain an anharmonic oscillator for [sup 148]Sm, a PES with two minima for [sup 150]Sm and a rotational PES for [sup 152]Sm. ((orig.))

  16. Validation of satellite-derived land surface variables - international coordination and status

    Science.gov (United States)

    Schaepman-Strub, Gabriela

    2015-04-01

    Validation and quality assessment are important components in the processing chain of satellite-derived land surface products. While most products nowadays are being validated by the responsible space agency, common validation data sets and methods across products from different agencies are still under development. The aim of the Land Product Validation Sub-group (Committee on Earth Observation Satellites) is to internationally coordinate intercomparison and validation efforts of satellite-derived land surface variables. Main components of the proposed validation concept are a peer-reviewed protocol describing standard methods and the identification of fiducial reference data and reference sites where new validation methods and algorithms can be tested. The identified methods, fiducial reference data, and satellite product subsets are then integrated in an online platform to generate standardized validation reports. This presentation summarizes the state of validation of satellite-derived products as assessed by LPV. LPV currently covers albedo, FAPAR, LAI, land cover, snow cover, land surface temperature, soil moisture, phenology, and fire/burnt area. For a selected set of above variables, a summary of validation methods, available in situ data, challenges, and validation stage are provided. We conclude with the identification of methodological gaps and data needs for a sustainable validation of satellite-based terrestrial Essential Climate and Biodiversity Variables in support of the climate observing system and biodiversity and ecosystem services assessments. The presentation is thought to highlight achievements by LPV, as well as to reach out to the satellite product user community and to measurement networks interested in supporting validation efforts with reference data.

  17. Cobalt(II phthalocyanine bonded to 3-n-propylimidazole immobilized on silica gel surface: preparation and electrochemical properties

    Directory of Open Access Journals (Sweden)

    Fujiwara Sergio T.

    1999-01-01

    Full Text Available Co-Phthalocyanine complex was immobilized on 3-n-propylimidazole groups grafted on a porous SiO2 surface (specific surface area S BET = 500 m² g-1 and efficiently electrocatalyzed the oxalic acid oxidation on a carbon paste electrode surface made of this material. Intermolecular interactions of the complex species which can normally interfere in the redox process practically are not observed in the present case because of a low average surface density, delta = 4.7 x 10-13 mol cm-2 (delta = Nf/S BET, where Nf is the amount of adsorbed Co-phtalocyanine per gram of modified silica gel of the complex species material prepared. The linear response of the electrode to oxalic acid concentration, between 6.5 x 10-4 and 3.2 x 10-3 mol L-1, associated with its high chemical stability makes the covalently immobilized Co-phtalocyanine complex material very attractive in preparing a new class of chemical sensors.

  18. Development of graphene oxide/poly(3,4-ethylenedioxythiophene)/poly(styrene sulfonate) thin film-based electrochemical surface plasmon resonance immunosensor for detection of human immunoglobulin G

    Science.gov (United States)

    Pothipor, Chammari; Lertvachirapaiboon, Chutiparn; Shinbo, Kazunari; Kato, Keizo; Kaneko, Futao; Ounnunkad, Kontad; Baba, Akira

    2018-02-01

    An electrochemically synthesized graphene oxide (GO)/poly(3,4-ethylenedioxythiophene) (PEDOT)/poly(styrene sulfonate) (PSS) thin film-based electrochemical surface plasmon resonance (EC-SPR) sensor chip was developed and employed for the detection of human immunoglobulin G (IgG). GO introduced the carboxylic group on the film surface, which also allowed electrochemical control, for the immobilization of the anti-IgG antibody via covalent bonding through amide coupling reaction. The SPR sensitivity of the detection was improved under the control by applying an electrochemical potential, by which the sensitivity was increased by the increment in applied potential. Among the open-circuit and different applied potentials in the range of ‑1.0 to 0.50 V, the EC-SPR immunosensor at an applied potential of 0.50 V exhibited the highest sensitivity of 6.08 × 10‑3 mL µg‑1 cm‑2 and linearity in the human IgG concentration range of 1.0 to 10 µg mL‑1 with a relatively low detection limit of 0.35 µg mL‑1. The proposed sensor chip is promising for immunosensing at the physiological level.

  19. Electrochemical cell

    Science.gov (United States)

    Nagy, Zoltan; Yonco, Robert M.; You, Hoydoo; Melendres, Carlos A.

    1992-01-01

    An electrochemical cell has a layer-type or sandwich configuration with a Teflon center section that houses working, reference and counter electrodes and defines a relatively narrow electrolyte cavity. The center section is surrounded on both sides with thin Teflon membranes. The membranes are pressed in place by a pair of Teflon inner frames which are in turn supported by a pair of outer metal frames. The pair of inner and outer frames are provided with corresponding, appropriately shaped slits that are in plane generally transverse to the plane of the working electrode and permit X-ray beams to enter and exit the cell through the Teflon membranes that cover the slits so that the interface between the working electrode and the electrolyte within the cell may be analyzed by transmission geometry. In one embodiment, the center section consists of two parts, one on top of the other. Alternatively, the center section of the electrochemical cell may consist of two intersliding pieces or may be made of a single piece of Teflon sheet material. The electrolyte cavity is shaped so that the electrochemical cell can be rotated 90.degree. in either direction while maintaining the working and counter electrodes submerged in the electrolyte.

  20. Bonding of anthracene derivatives to a Cu (111) surface: a combined STM and DFT study

    Science.gov (United States)

    Wyrick, Jonathan; Zhu, Yeming; Salib, Daniel; Holzke, Connor; Cheng, Zhihai; Bartels, Ludwig

    2013-03-01

    We compare and contrast three anthracene derivatives whose 9,10 hydrogens are replaced by the elements O, S, and Se respectively that act as ``feet'' binding the molecules to a Cu (111) substrate. DFT calculations are compared with and shed light on STM data for the three molecules. We analyze the three species in terms of their geometric and electronic structure upon adsorption, taking into account the competing effects that the ``feet'' have with the anthracene moiety in their interactions with the underlying Cu surface. At the time of contributed research, Zhihai was at University of California at Riverside

  1. Variability of basin scale water resources indicators derived from global hydrological and land surface models

    Science.gov (United States)

    Werner, Micha; Blyth, Eleanor; Schellekens, Jaap

    2016-04-01

    Global hydrological and land-surface models are becoming increasingly available, and as the resolution of these improves, as well how hydrological processes are represented, so does their potential. These offer consistent datasets at the global scale, which can be used to establish water balances and derive policy relevant indicators in medium to large basins, including those that are poorly gauged. However, differences in model structure, model parameterisation, and model forcing may result in quite different indicator values being derived, depending on the model used. In this paper we explore indicators developed using four land surface models (LSM) and five global hydrological models (GHM). Results from these models have been made available through the Earth2Observe project, a recent research initiative funded by the European Union 7th Research Framework. All models have a resolution of 0.5 arc degrees, and are forced using the same WATCH-ERA-Interim (WFDEI) meteorological re-analysis data at a daily time step for the 32 year period from 1979 to 2012. We explore three water resources indicators; an aridity index, a simplified water exploitation index; and an indicator that calculates the frequency of occurrence of root zone stress. We compare indicators derived over selected areas/basins in Europe, Colombia, Southern Africa, the Indian Subcontinent and Australia/New Zealand. The hydrological fluxes calculated show quite significant differences between the nine models, despite the common forcing dataset, with these differences reflected in the indicators subsequently derived. The results show that the variability between models is related to the different climates types, with that variability quite logically depending largely on the availability of water. Patterns are also found in the type of models that dominate different parts of the distribution of the indicator values, with LSM models providing lower values, and GHM models providing higher values in some

  2. Labeling Cell Surface GPIs and GPI-Anchored Proteins through Metabolic Engineering with Artificial Inositol Derivatives.

    Science.gov (United States)

    Lu, Lili; Gao, Jian; Guo, Zhongwu

    2015-08-10

    Glycosylphosphatidylinositol (GPI) anchoring of proteins to the cell surface is important for various biological processes, but GPI-anchored proteins are difficult to study. An effective strategy was developed for the metabolic engineering of cell-surface GPIs and GPI-anchored proteins by using inositol derivatives carrying an azido group. The azide-labeled GPIs and GPI-anchored proteins were then tagged with biotin on live cells through a click reaction, which allows further elaboration with streptavidin-conjugated dyes or other molecules. The strategy can be used to label GPI-anchored proteins with various tags for biological studies. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  3. Surface Markers for Chondrogenic Determination: A Highlight of Synovium-Derived Stem Cells

    Directory of Open Access Journals (Sweden)

    Douglas D. Campbell

    2012-11-01

    Full Text Available Cartilage tissue engineering is a promising field in regenerative medicine that can provide substantial relief to people suffering from degenerative cartilage disease. Current research shows the greatest chondrogenic potential for healthy articular cartilage growth with minimal hypertrophic differentiation to be from mesenchymal stem cells (MSCs of synovial origin. These stem cells have the capacity for differentiation into multiple cell lineages related to mesenchymal tissue; however, evidence exists for cell surface markers that specify a greater potential for chondrogenesis than other differentiation fates. This review will examine relevant literature to summarize the chondrogenic differentiation capacities of tested synovium-derived stem cell (SDSC surface markers, along with a discussion about various other markers that may hold potential, yet require further investigation. With this information, a potential clinical benefit exists to develop a screening system for SDSCs that will produce the healthiest articular cartilage possible.

  4. Enhancing the Bioconversion of Azelaic Acid to Its Derivatives by Response Surface Methodology

    Directory of Open Access Journals (Sweden)

    Nurshafira Khairudin

    2018-02-01

    Full Text Available Azelaic acid (AzA and its derivatives have been known to be effective in the treatment of acne and various cutaneous hyperpigmentary disorders. The esterification of azelaic acid with lauryl alcohol (LA to produce dilaurylazelate using immobilized lipase B from Candida antarctica (Novozym 435 is reported. Response surface methodology was selected to optimize the reaction conditions. A well-fitting quadratic polynomial regression model for the acid conversion was established with regards to several parameters, including reaction time and temperature, enzyme amount, and substrate molar ratios. The regression equation obtained by the central composite design of RSM predicted that the optimal reaction conditions included a reaction time of 360 min, 0.14 g of enzyme, a reaction temperature of 46 °C, and a molar ratio of substrates of 1:4.1. The results from the model were in good agreement with the experimental data and were within the experimental range (R2 of 0.9732.The inhibition zone can be seen at dilaurylazelate ester with diameter 9.0±0.1 mm activities against Staphylococcus epidermidis S273. The normal fibroblasts cell line (3T3 was used to assess the cytotoxicity activity of AzA and AzA derivative, which is dilaurylazelate ester. The comparison of the IC50 (50% inhibition of cell viability value for AzA and AzA derivative was demonstrated. The IC50 value for AzA was 85.28 μg/mL, whereas the IC50 value for AzA derivative was more than 100 μg/mL. The 3T3 cell was still able to survive without any sign of toxicity from the AzA derivative; thus, it was proven to be non-toxic in this MTT assay when compared with AzA.

  5. Electrochemical biofilm control: A review

    Science.gov (United States)

    Sultana, Sujala T; Babauta, Jerome T; Beyenal, Haluk

    2015-01-01

    One of the methods of controlling biofilms that has widely been discussed in the literature is to apply a potential or electrical current to a metal surface on which the biofilm is growing. Although electrochemical biofilm control has been studied for decades, the literature is often conflicting, as is detailed in this review. The goals of this review are to (1) present the current status of knowledge regarding electrochemical biofilm control, (2) establish a basis for a fundamental definition of electrochemical biofilm control and requirements for studying it, (3) discuss current proposed mechanisms, and (4) introduce future directions in the field. It is expected that the review will provide researchers with guidelines on comparing data sets across the literature and generating comparable data sets. The authors believe that, with the correct design, electrochemical biofilm control has great potential for industrial use. PMID:26592420

  6. Tailoring the morphology and electrocatalytic properties of electrochemically formed Ag/TiO2 composite deposits on titanium surfaces

    Directory of Open Access Journals (Sweden)

    S. V. MENTUS

    2007-12-01

    Full Text Available Three different forms of Ag/TiO2 composite layers, which have whisker-, dot- and island-like distribution of silver were obtained on a mechanically polished titanium surface by adjusting the conditions of silver deposition from an aqueous AgNO3 solution. The deposit morphology was the result of both the program of electrode polarization and the template action of the simultaneously formed TiO2 layer. The catalytic activity of the composite layers toward the oxygen reduction reaction was studied in aqueous 0.1 M NaOH solutions and found to be a function of both the surface loading of silver and the type of silver distribution within the Ag/TiO2 composite layers. The reaction path of oxygen reduction on the composite layers was found to be always a 4e- one, characteristic otherwise of polycrystalline silver electrodes.

  7. Effect of Vegetation Patterns on SAR derived Surface Soil Moisture Distribution

    Science.gov (United States)

    Koyama, C. N.; Schneider, K.

    2012-12-01

    conditions, are used to derive biomass information independently from the soil moisture retrieval. Nevertheless, the canopy still has an attenuation effect on the co-polarized backscattering, but this can be corrected by using the vegetation information obtained from the other SAR observables. For constant permittivity states of the soil surface the canopy can have a disturbing effect of up to 6dB. This is the same order of magnitude of dynamic range as observed for soil moisture values ranging from 10 - 40 Vol.-% over bare surfaces. The present study is focused on the Rur catchment (Germany) where the effect of different vegetation patterns on the spatial distribution of near-surface soil water content is investigated by comparison between ALOS PALSAR derived biomass and soil moisture maps. The findings show that the impact of vegetation on the near-surface moisture contents may vary considerably. For wet and intermediate soil conditions where enough water is available for transpiration it was observed that the near-surface moisture content tends to be higher on vegetated fields. This may be explained by the fact that the canopy hampers evaporations due to lack of air movement while the plants uptake water from deeper soil layers. However if the water supply is low the plant water consumption can also lead to accelerated drying of the soil surface. This was especially observed for cereal crops.

  8. A new CM SAF Solar Surface Radiation Climate Data Set derived from Meteosat Satellite Observations

    Science.gov (United States)

    Trentmann, J.; Mueller, R. W.; Pfeifroth, U.; Träger-Chatterjee, C.; Cremer, R.

    2014-12-01

    The incoming surface solar radiation has been defined as an essential climate variable by GCOS. It is mandatory to monitor this part of the earth's energy balance, and thus gain insights on the state and variability of the climate system. In addition, data sets of the surface solar radiation have received increased attention over the recent years as an important source of information for the planning of solar energy applications. The EUMETSAT Satellite Application Facility on Climate Monitoring (CM SAF) is deriving surface solar radiation from geostationary and polar-orbiting satellite instruments. While CM SAF is focusing on the generation of high-quality long-term climate data records, also operationally data is provided in short time latency within 8 weeks. Here we present SARAH (Solar Surface Radiation Dataset - Heliosat), i.e. the new CM SAF Solar Surface Radiation data set based on Meteosat satellite observations. SARAH provides instantaneous, daily- and monthly-averaged data of the effective cloud albedo (CAL), the direct normalized solar radiation (DNI) and the solar irradiance (SIS) from 1983 to 2013 for the full view of the Meteosat satellite (i.e, Europe, Africa, parts of South America, and the Atlantic ocean). The data sets are generated with a high spatial resolution of 0.05 deg allowing for detailed regional studies, and are available in netcdf-format at no cost without restrictions at www.cmsaf.eu. We provide an overview of the data sets, including a validation against reference measurements from the BSRN and GEBA surface station networks.

  9. Effect of Amine Adlayer on Electrochemical Uric Acid Sensor Conducted on Electrochemically Reduced Graphene Oxide

    Energy Technology Data Exchange (ETDEWEB)

    Park, Sumi; Kim, Kyuwon [Incheon National University, Incheon (Korea, Republic of)

    2016-03-15

    The electrochemical biosensing efficiency of uric acid (UA) detection on an electrochemically reduced graphene oxide (ERGO)-decorated electrode surface was studied by using various amine linkers used to immobilize ERGO. The amine linkers aminoethylphenyldiazonium , 2,2'-(ethylenedioxy)bis(ethylamine), 3-aminopro-pyltriethoxysilane, and polyethyleneimine were coated on indium-tin-oxide electrode surfaces through chemical or electrochemical deposition methods. ERGO-decorated surfaces were prepared by the electrochemical reduction of graphene oxide (GO), which was immobilized on the amine-coated electrode surfaces through the electrostatic interaction between GO and the ammonium ion of the linker on the surface. We monitored the sensing results of electrochemical UA detection with differential pulse voltammetry. The ERGO-modified surface presented electrocatalytic oxidation of UA and ascorbic acid. Among the different amines tested, 3-aminopropyltriethoxysilane provided the best biosensing performance in terms of sensitivity and reproducibility.

  10. Immobilization of nanobeads on a surface to control the size, shape and distribution of pores in electrochemically generated sol-gel films

    Science.gov (United States)

    Ciabocco, Michela; Berrettoni, Mario; Zamponi, Silvia

    2015-01-01

    Electrochemically assisted deposition of an ormosil film at a potential where hydrogen ion is generated as the catalyst yields insulating films on electrodes. When the base electrode is modified with 20-nm poly(styrene sulfonate), PSS, beads bound to the surface with 3-aminopropyltriethoxysilane (APTES) and using (CH3)3SiOCH3 as the precursor, the resulting film of organically modified silica (ormosil) has cylindrical channels that reflect both the diameter of the PSS and the distribution of the APTES-PSS on the electrode. At an electrode modified by a 20-min immersion in 0.5 mmol dm-3 APTES followed by a 30-s immersion in PSS, a 20-min electrolysis at 1.5 V in acidified (CH3)3SiOCH3 resulted in an ormosil film with 20-nm pores separated by 100 nm. Cyclic voltammetry of Ru(CN)64- at scan rates above 5 mVs-1 yielded currents controlled primarily by linear diffusion. Below 5 mVs-1, convection rather than the expected factor, radial diffusion, apparently limited the current. PMID:26167128

  11. Relationship between the specific surface area of rust and the electrochemical behavior of rusted steel in a wet-dry acid corrosion environment

    Science.gov (United States)

    Liu, Wei; Zhao, Qing-he; Li, Shuan-zhu

    2017-01-01

    The relationship between the specific surface area (SSA) of rust and the electrochemical behavior of rusted steel under wet-dry acid corrosion conditions was investigated. The results showed that the corrosion current density first increased and then decreased with increasing SSA of the rust during the corrosion process. The structure of the rust changed from single-layer to double-layer, and the γ-FeOOH content decreased in the inner layer of the rust with increasing corrosion time; by contrast, the γ-FeOOH content in the outer layer was constant. When the SSA of the rust was lower than the critical SSA corresponding to the relative humidity during the drying period, condensed water in the micropores of the rust could evaporate, which prompted the diffusion of O2 into the rust and the following formation process of γ-FeOOH, leading to an increase of corrosion current density with increasing corrosion time. However, when the SSA of the rust reached or exceeded the critical SSA, condensate water in the micro-pores of the inner layer of the rust could not evaporate which inhibited the diffusion of O2 and decreased the γ-FeOOH content in the inner rust, leading to a decrease of corrosion current density with increasing corrosion time.

  12. Electrode structure analysis and surface characterization for lithium-ion cells simulated low-Earth-orbit satellite operation. I. Electrochemical behavior and structure analysis

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Xianming; Yamada, Chisa; Naito, Hitoshi; Segami, Go; Kibe, Kouichi [Institute of Space Technology and Aeronautics, Japan Aerospace Exploration Agency, Tsukuba Space Center, Sengen 2-1-1, Ibaraki 305-8505 (Japan); Sakiyama, Yoko; Takahashi, Yoshikazu; Hironaka, Toshiya; Hayashi, Eiji [Toray Research Center, Inc., Sonoyama 3-3-7, Otsu, Shiga 520-8567 (Japan)

    2007-05-01

    Lithium-ion cells for satellite applications operate under a special condition, and are expected to behave differently from those for commercial purposes. To understand the performance-degradation mechanism of lithium-ion cells experienced cycle-life testing in a simulated low-Earth-orbit (LEO) satellite operation, we conducted the structure analysis and surface characterization of the aged LiCoO{sub 2} cathode and graphite anode obtained from a lithium-ion cell with 4350-cycle LEO simulation experience. The analysis results were compared with a fresh cell which served as control. This paper provides a review of testing results on electrochemical and structure analysis. The capacity-verification and impedance measure results indicated that the LiCoO{sub 2} cathode, rather than graphite anode, was responsible for the performance degradation of the aged cell. This conclusion was confirmed by the structure analysis. The qualitative analysis of the XRD spectra disclosed that the aged cathode exhibited a much larger structure change than the aged anode. We also detected the lithium ions that were irreversibly reserved in graphite anode in XRD and {sup 7}Li nuclear magnetic resonance (NMR) analysis of aged graphite anode. These results lead us to deduce that the serious structure change in LiCoO{sub 2} cathode was primarily responsible for the performance degradation of the aged cell. (author)

  13. UV and gamma irradiation effects on surface properties of polyurethane derivative from castor oil

    Energy Technology Data Exchange (ETDEWEB)

    Azevedo, Elaine C.; Nascimento, Eduardo M., E-mail: helunica@yahoo.com.br [Universidade Tecnologica Federal do Parana (UTFPR), Curitiba, PR (Brazil); Chierice, Gilberto O.; Claro Neto, Salvador [Universidade de Sao Paulo (IQSC/USP), Sao Carlos, SP (Brazil). Instituto de Quimica; Lepienski, Carlos M. [Universidade Federal do Parana (UFPR), Curitiba (Brazil)

    2013-07-01

    Gamma and ultraviolet radiation effects on hardness, elastic modulus and viscoelastic properties of polyurethane derived from castor oil (PU) were investigated by nanoindentation tests. Modifications on surface morphology, induce by radiation, were observed by atomic force microscopy. The polyurethane derivative from castor oil shows good resistance to gamma radiation, with only small changes in hardness, elastic modulus, viscoelastic properties and contact angle. The hardness of PY increases at the near surface region due to UVA radiation and decreases after UVC radiation. The contact angle for water drop decreases after UVC radiation, by not after gamma radiation, despite a significant increase in roughness. Such results are attributed to different responses from polyurethane to radiation energy. Increase in hardness due to UVA is attributed to a higher crosslinking at shallow depths, while a decrease in mechanical properties may be attributed to chain scission. These results are consistent with the modifications on viscoelastic properties. Shore D hardness did not show the same trend as observed by nanoindentation results. Hardness, viscoelastic properties and contact angle of castor oil polyurethane are more severely influenced by UVC radiation, while gamma radiation does not have a significant effect. (author)

  14. First Derivative UV Spectra of Surface Water as a Monitor of Chlorination in Drinking Water Treatment

    Directory of Open Access Journals (Sweden)

    V. Zitko

    2001-01-01

    Full Text Available Many countries require the presence of free chlorine at about 0.1 mg/l in their drinking water supplies. For various reasons, such as cast-iron pipes or long residence times in the distribution system, free chlorine may decrease below detection limits. In such cases it is important to know whether or not the water was chlorinated or if nonchlorinated water entered the system by accident. Changes in UV spectra of natural organic matter in lakewater were used to assess qualitatively the degree of chlorination in the treatment to produce drinking water. The changes were more obvious in the first derivative spectra. In lakewater, the derivative spectra have a maximum at about 280 nm. This maximum shifts to longer wavelengths by up to 10 nm, decreases, and eventually disappears with an increasing dose of chlorine. The water treatment system was monitored by this technique for over 1 year and changes in the UV spectra of water samples were compared with experimental samples treated with known amounts of chlorine. The changes of the UV spectra with the concentration of added chlorine are presented. On several occasions, water, which received very little or no chlorination, may have entered the drinking water system. The results show that first derivative spectra are potentially a tool to determine, in the absence of residual chlorine, whether or not surface water was chlorinated during the treatment to produce potable water.

  15. Evaluation of altimetry‐derived surface current products using Lagrangian drifter trajectories in the eastern Gulf of Mexico

    National Research Council Canada - National Science Library

    Liu, Yonggang; Weisberg, Robert H; Vignudelli, Stefano; Mitchum, Gary T

    2014-01-01

    Lagrangian particle trajectory models based on several altimetry‐derived surface current products are used to hindcast the drifter trajectories observed in the eastern Gulf of Mexico during May to August 2010...

  16. Massachusetts Bay - Internal wave packets digitized from SAR imagery and intersected with a bathymetrically derived slope surface

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — This feature class contains internal wave packets digitized from SAR imagery and intersected with a bathymetrically derived slope surface for Massachusetts Bay. The...

  17. Western Arctic Coastal Plain, IFSAR-derived, Digital Surface Model. University of Alaska Fairbanks, Geophysical Institute Permafrost Laboratory (2013).

    Data.gov (United States)

    Arctic Landscape Conservation Cooperative — This dataset consists of a mosaic created from an Interferometric Synthetic Aperture Radar (IfSAR) derived digital surface model (DSM) acquired over the National...

  18. Potential of Multitemporal Tandem-X Derived Crop Surface Models for Maize Growth Monitoring

    Science.gov (United States)

    Hütt, C.; Tilly, N.; Schiedung, H.; Bareth, G.

    2016-06-01

    In this study, first results of retrieving plant heights of maize fields from multitemporal TanDEM-X images are shown. Three TanDEM-X dual polarization spotlight acquisitions were taken over a rural area in Germany in the growing season 2014. By interferometric processing, digital terrain models (DTM) were derived for each date with 5m resolution. From the data of the first acquisition (June 1st) taken before planting, a DTM of the bare ground is generated. The data of the following acquisition dates (July 15th, July 26th) are used to establish crop surface models (CSM). A CSM represents the crop surface of a whole field in a high resolution. By subtracting the DTM of the ground from each CSM, the actual plant height is calculated. Within these data sets 30 maize fields in the area of interest could be detected and verified by external land use data. Besides the spaceborne measurements, one of the maize fields was intensively investigated using terrestrial laser scanning (TLS), which was carried out at the same dates as the predicted TanDEM-X acquisitions. Visual inspection of the derived plant heights, and accordance of the individually processed polarisations over the maize fields, demonstrate the feasibility of the proposed method. Unfortunately, the infield variability of the intensively monitored field could not be successfully captured in the TanDEM-X derived plant heights and merely the general trend is visible. Nevertheless, the study shows the potential of the TanDEM-X constellation for maize height monitoring on field level.

  19. A comparison of optical and microwave scintillometers with eddy covariance derived surface heat fluxes

    KAUST Repository

    Yee, Mei Sun

    2015-11-01

    Accurate measurements of energy fluxes between land and atmosphere are important for understanding and modeling climatic patterns. Several methods are available to measure heat fluxes, and scintillometers are becoming increasingly popular because of their ability to measure sensible (. H) and latent (. LvE) heat fluxes over large spatial scales. The main motivation of this study was to test the use of different methods and technologies to derive surface heat fluxes.Measurements of H and LvE were carried out with an eddy covariance (EC) system, two different makes of optical large aperture scintillometers (LAS) and two microwave scintillometers (MWS) with different frequencies at a pasture site in a semi-arid environment of New South Wales, Australia. We used the EC measurements as a benchmark. Fluxes derived from the EC system and LAS systems agreed (R2>0.94), whereas the MWS systems measured lower H (bias ~60Wm-2) and larger LvE (bias ~65Wm-2) than EC. When the scintillometers were compared against each other, the two LASs showed good agreement of H (R2=0.98), while MWS with different frequencies and polarizations led to different results. Combination of LAS and MWS measurements (i.e., two wavelength method) resulted in performance that fell in between those estimated using either LAS or MWS alone when compared with the EC system. The cause for discrepancies between surface heat fluxes derived from the EC system and those from the MWS systems and the two-wavelength method are possibly related to inaccurate assignment of the structure parameter of temperature and humidity. Additionally, measurements from MWSs can be associated with two values of the Bowen ratio, thereby leading to uncertainties in the estimation of the fluxes. While only one solution has been considered in this study, when LvE was approximately less than 200Wm-2, the alternate solution may be more accurate. Therefore, for measurements of surface heat fluxes in a semi-arid or dry environment, the

  20. Determination of the mechanism and extent of surface degradation in Ni-based cathode materials after repeated electrochemical cycling

    Directory of Open Access Journals (Sweden)

    Sooyeon Hwang

    2016-09-01

    Full Text Available We take advantage of scanning transmission electron microscopy and electron energy loss spectroscopy to investigate the changes in near-surface electronic structure and quantify the degree of local degradation of Ni-based cathode materials with the layered structure (LiNi0.8Mn0.1Co0.1O2 and LiNi0.4Mn0.3Co0.3O2 after 20 cycles of delithiation and lithiation. Reduction of transition metals occurs in the near-surface region of cathode materials: Mn is the major element to be reduced in the case of relatively Mn-rich composition, while reduction of Ni ions is dominant in Ni-rich materials. The valences of Ni and Mn ions are complementary, i.e., when one is reduced, the other is oxidized in order to maintain charge neutrality. The depth of degradation zone is found to be much deeper in Ni-rich materials. This comparative analysis provides important insights needed for the devising of new cathode materials with high capacity as well as long lifetime.

  1. Endothelial cell surface heparan sulfate (ESHS) and synthetic heparin derivatives as hemocompatible coating for biomaterials

    Energy Technology Data Exchange (ETDEWEB)

    Hoffmann, M.; Huppertz, B.; Horres, R.; Baumann, H. [RWTH, Aachen (Germany). Makromolekulare Chemie und Textilchemie, Haemokompatible und Biokompatible Biomaterialien; Keller, R. [Klinische Anstalten der Stadt Koeln (Germany)

    2001-02-01

    In the present overview a coating procedure, that has been developed in our working group for medical devices e.g. implants, which are exposed to permanent blood contact and therefore have to fulfill the highest standard of hemocompatibility is described. For this purpose an endothelial cell surface heparansulfate, which belongs to the class of glycosaminoglycans is used as coating substance. This substance can be isolated from endothelial cell culture, tissue extracts or organ perfusates. Alternatively chemical regio- and stereoselective modified derivatives of the structurally related anticoagulant heparin were brought to action. These substances are anchored covalently or ionically by application of a wide spectrum of immobilization techniques on many different material surfaces. Polymer materials modified as described here have been tested for hemocompatibility in invitro and in invivo experiments with Austrian sheep. The results show, that the described method is an advanced solution for the creation of long term hemocompatible artificial material surfaces. (orig.) [German] In dem vorliegenden Uebersichtsartikel wird ein in unserer Arbeitsgruppe entwickeltes athrombogenes und plaettcheninertes Beschichtungsverfahren fuer medizinische Werkstoffoberflaechen wie z.B. Implantate, die staendigem direktem Blutkontakt ausgesetzt sind und infolge dessen ein Hoechstmass an Haemokompatibilitaet aufweisen muessen, zusammenfassend beschrieben. Hierzu wird als Beschichtungssubstanz ein aus Zellkultur, Gewebeextrakten oder Organperfusaten isolierbares zur Klasse der Glycosaminoglycane zaehlendes Endothelzelloberflaechenparansulfat (ESHS) verwendet. Alternativ werden chemisch regio- und stereoselektiv modifizierte Derivate des strukturverwandten klassischen Antikoagulanzes Heparin als Beschichtungssubstanz eingesetzt. Diese Substanzen werden unter Anwendung eines breiten Spektrums von Immobilisierungstechniken auf verschiedensten Werkstoffoberflaechen kovalent oder ionisch

  2. Fabrication of Superhydrophobic Metal Surfaces with Self-Assembled Monolayers of Silane Derivatives Having Inter-Hydrogen Bonding

    Energy Technology Data Exchange (ETDEWEB)

    Park, Yeon Hwa; Han, Moon Hee; Ahn, Yong Hyun [Dankook University, Yongin (Korea, Republic of)

    2011-03-15

    In this study, we synthesized hexyl- and phenethyl-urea silanes and used them in the fabrication of superhydro-phobic surfaces on cupper deposited magnesium plates. This method is simple and cheap; in addition, the superhydro-phobic surfaces obtained were stable over a wide range of pH values. Thus, the silane derivatives synthesized in this study can serve as suitable alternatives to low surface energy materials such as fluorinated alkyl silane derivatives used in the fabrication of superhydrophobic surfaces. In recent times, there has been an increasing interest in superhydrophobic surfaces, as these surfaces have applications in various fields. Many different methods for the fabrication of superhydrophobic surfaces have been reported; these include a sol-gel method, chemical etching, the application of a polymer, electrodeposition, and the use of self-assembled monolayers (SAMs) of organic materials.

  3. Kinetics of the electrochemically-assisted deposition of sol-gel films.

    Science.gov (United States)

    Liu, Liang; Walcarius, Alain

    2017-06-14

    Electrochemically-assisted deposition is now becoming a widespread method for preparing sol-gel films. It is based on the electrochemical generation of OH - ions, which can then catalyze the sol-gel condensation reactions. It has a key advantage of selectively facilitating the film deposition on electrochemically active surfaces while not affecting the stability of the bulk precursor solution. Experimental studies have clearly shown that the thickness of the electrochemically-assisted deposited films is influenced by the deposition parameters such as the potential and time. However, there is still a lack of quantitative description of the kinetics of film growth due to the complexity of the process. In this preliminary study, we derived quantitative analytical expressions for describing the kinetics associated with the growth of sol-gel films generated by electrochemically assisted deposition. Both heterogeneous and homogeneous condensation reactions were considered. The key strategy was to simplify the process by separating the electrochemical step of generating OH - ions with the condensation steps of film formation under approximation. Furthermore, numerical simulation was carried out to examine the validity and any errors in the analytical expressions in the cases when the required approximations were not fulfilled. The analytical expressions could well explain the trends observed in the experimental studies and could also be used for fitting the experimental results from the literature. This study provides a deeper understanding of the mechanism and quantitative guidance for manipulating electrochemically-assisted deposition processes at a large scale in industry. It may also be referred to in regard to other indirect electrodeposition systems in which the deposition is not an electrochemical step but is instead driven by electrochemically-generated catalysts.

  4. Correlations between the electrochemical behaviour and surface film composition of TZM alloy exposed to divertor water coolant environments

    Energy Technology Data Exchange (ETDEWEB)

    Maday, M.-F. [ENEA-CRE-Casaccia, Rome (Italy). Div. Nuovi Mater.; Giorgi, R. [ENEA-CRE-Casaccia, Rome (Italy). Div. Nuovi Mater.; Dikonimos-Makris, T. [ENEA-CRE-Casaccia, Rome (Italy). Div. Nuovi Mater.

    1997-07-01

    X-ray photoelectron spectroscopy (XPS) has been carried out on TZM alloy surfaces after short and long immersion tests in high temperature (250 C) aqueous environments simulating possible fusion reactor coolant conditions during operation. Phase identification by XPS was used in connection with the open circuit potential trends to suggest plausible hypotheses about TZM corrosion behaviour in the various chemical environments considered in this study. It was proposed that exposure of TZM to oxidizing water conditions produced poorly protective layers, which consist essentially of low (IV) and intermediate (V) valency Mo oxides/hydroxides. Conversely the results obtained in deaerated and reducing water conditions suggested that barrier films could develop in these environments: the phases exhibit a bilayered structure and consisted of an inner tetravalent Mo oxide/hydroxide and an outer hexavalent Mo oxide. The protective properties of such layers were attributed to the hexavalent Mo species. (orig.).

  5. A Novel Fiber Optic Surface Plasmon Resonance Biosensors with Special Boronic Acid Derivative to Detect Glycoprotein

    Directory of Open Access Journals (Sweden)

    Yang Zhang

    2017-10-01

    Full Text Available We proposed and demonstrated a novel tilted fiber Bragg grating (TFBG-based surface plasmon resonance (SPR label-free biosensor via a special boronic acid derivative to detect glycoprotein with high sensitivity and selectivity. TFBG, as an effective sensing element for optical sensing in near-infrared wavelengths, possess the unique capability of easily exciting the SPR effect on fiber surface which coated with a nano-scale metal layer. SPR properties can be accurately detected by measuring the variation of transmitted spectra at optical communication wavelengths. In our experiment, a 10° TFBG coated with a 50 nm gold film was manufactured to stimulate SPR on a sensor surface. To detect glycoprotein selectively, the sensor was immobilized using designed phenylboronic acid as the recognition molecule, which can covalently bond with 1,2- or 1,3-diols to form five- or six-membered cyclic complexes for attaching diol-containing biomolecules and proteins. The phenylboronic acid was synthetized with long alkyl groups offering more flexible space, which was able to improve the capability of binding glycoprotein. The proposed TFBG-SPR sensors exhibit good selectivity and repeatability with a protein concentration sensitivity up to 2.867 dB/ (mg/mL and a limit of detection (LOD of 15.56 nM.

  6. Electrochemical attosyringe

    Science.gov (United States)

    Laforge, François O.; Carpino, James; Rotenberg, Susan A.; Mirkin, Michael V.

    2007-01-01

    The ability to manipulate ultrasmall volumes of liquids is essential in such diverse fields as cell biology, microfluidics, capillary chromatography, and nanolithography. In cell biology, it is often necessary to inject material of high molecular weight (e.g., DNA, proteins) into living cells because their membranes are impermeable to such molecules. All techniques currently used for microinjection are plagued by two common problems: the relatively large injector size and volume of injected fluid, and poor control of the amount of injected material. Here we demonstrate the possibility of electrochemical control of the fluid motion that allows one to sample and dispense attoliter-to-picoliter (10−18 to 10−12 liter) volumes of either aqueous or nonaqueous solutions. By changing the voltage applied across the liquid/liquid interface, one can produce a sufficient force to draw solution inside a nanopipette and then inject it into an immobilized biological cell. A high success rate was achieved in injections of fluorescent dyes into cultured human breast cells. The injection of femtoliter-range volumes can be monitored by video microscopy, and current/resistance-based approaches can be used to control injections from very small pipettes. Other potential applications of the electrochemical syringe include fluid dispensing in nanolithography and pumping in microfluidic systems. PMID:17620612

  7. Electrochemical attosyringe.

    Science.gov (United States)

    Laforge, François O; Carpino, James; Rotenberg, Susan A; Mirkin, Michael V

    2007-07-17

    The ability to manipulate ultrasmall volumes of liquids is essential in such diverse fields as cell biology, microfluidics, capillary chromatography, and nanolithography. In cell biology, it is often necessary to inject material of high molecular weight (e.g., DNA, proteins) into living cells because their membranes are impermeable to such molecules. All techniques currently used for microinjection are plagued by two common problems: the relatively large injector size and volume of injected fluid, and poor control of the amount of injected material. Here we demonstrate the possibility of electrochemical control of the fluid motion that allows one to sample and dispense attoliter-to-picoliter (10(-18) to 10(-12) liter) volumes of either aqueous or nonaqueous solutions. By changing the voltage applied across the liquid/liquid interface, one can produce a sufficient force to draw solution inside a nanopipette and then inject it into an immobilized biological cell. A high success rate was achieved in injections of fluorescent dyes into cultured human breast cells. The injection of femtoliter-range volumes can be monitored by video microscopy, and current/resistance-based approaches can be used to control injections from very small pipettes. Other potential applications of the electrochemical syringe include fluid dispensing in nanolithography and pumping in microfluidic systems.

  8. Derivation of the Wenzel and Cassie Equations from a Phase Field Model for Two Phase Flow on Rough Surface

    KAUST Repository

    Xu, Xianmin

    2010-01-01

    In this paper, the equilibrium behavior of an immiscible two phase fluid on a rough surface is studied from a phase field equation derived from minimizing the total free energy of the system. When the size of the roughness becomes small, we derive the effective boundary condition for the equation by the multiple scale expansion homogenization technique. The Wenzel and Cassie equations for the apparent contact angles on the rough surfaces are then derived from the effective boundary condition. The homogenization results are proved rigorously by the F-convergence theory. © 2010 Society for Industrial and Applied Mathematics.

  9. Synthesis, pH dependent photometric and electrochemical investigation, redox mechanism and biological applications of novel Schiff base and its metallic derivatives

    Science.gov (United States)

    Rauf, Abdur; Shah, Afzal; Khan, Abdul Aziz; Shah, Aamir Hassan; Abbasi, Rashda; Qureshi, Irfan Zia; Ali, Saqib

    2017-04-01

    A novel Schiff base, 1-((2, 4-dimethylphenylimino)methyl)naphthalen-2-ol abbreviated as (HL) and its four metallic complexes were synthesized and confirmed by 1H and 13C NMR, FTIR, TGA and UV-Visible spectroscopy. Schiff base was also characterized by X-ray analysis. The photometric and electrochemical responses of all the synthesized compounds were investigated in a wide pH range. Structures of the compounds were optimized computationally for the evaluation of different physico-chemical parameters. On the basis of electrochemical results the redox mechanistic pathways of the compounds were proposed. The cytotoxicity analysis on Hela cells revealed that HL and its complexes inhibit cell growth as revealed from their IC50 values (HL):106.7 μM, (L2VO): 40.66 μM, (L2Sn): 5.92 μM, (L2Zn): 42.82 and (L2Co): 107.68 μM. The compounds were tested for anti-diabetic, triglyceride, cholesterol, anti-microbial, anti-fungal and enzyme inhibition activities. The results revealed that HL and its complexes are promising new therapeutic options as these compounds exhibit strong activity against cancer cells, diabetics, fungal and microbial inhibition.

  10. Synthesis, pH dependent photometric and electrochemical investigation, redox mechanism and biological applications of novel Schiff base and its metallic derivatives.

    Science.gov (United States)

    Rauf, Abdur; Shah, Afzal; Khan, Abdul Aziz; Shah, Aamir Hassan; Abbasi, Rashda; Qureshi, Irfan Zia; Ali, Saqib

    2017-04-05

    A novel Schiff base, 1-((2, 4-dimethylphenylimino)methyl)naphthalen-2-ol abbreviated as (HL) and its four metallic complexes were synthesized and confirmed by 1H and 13C NMR, FTIR, TGA and UV-Visible spectroscopy. Schiff base was also characterized by X-ray analysis. The photometric and electrochemical responses of all the synthesized compounds were investigated in a wide pH range. Structures of the compounds were optimized computationally for the evaluation of different physico-chemical parameters. On the basis of electrochemical results the redox mechanistic pathways of the compounds were proposed. The cytotoxicity analysis on Hela cells revealed that HL and its complexes inhibit cell growth as revealed from their IC50 values (HL):106.7μM, (L2VO): 40.66μM, (L2Sn): 5.92μM, (L2Zn): 42.82 and (L2Co): 107.68μM. The compounds were tested for anti-diabetic, triglyceride, cholesterol, anti-microbial, anti-fungal and enzyme inhibition activities. The results revealed that HL and its complexes are promising new therapeutic options as these compounds exhibit strong activity against cancer cells, diabetics, fungal and microbial inhibition. Copyright © 2017 Elsevier B.V. All rights reserved.

  11. Materials based on carbon-filled porous layers of PVC cyclam derivatives cross-linked with the surfaces of asbestos fabric fibers

    Science.gov (United States)

    Tzivadze, A. Yu.; Fridman, A. Ya.; Morozova, E. M.; Sokolova, N. P.; Voloshchuk, A. M.; Petukhova, G. A.; Bardishev, I. I.; Gorbunov, A. M.; Novikov, A. K.; Polyakova, I. Ya.; Titova, V. N.; Yavich, A. A.; Petrova, N. V.

    2016-08-01

    The synthesis of bilayer materials with porous upper layers composed of PVC hydroxyethylcyclam derivatives filled with carbon and a layer consisting of hydroxyethylcyclam, cross-linked via Si-O-C groups with the silica chains of a developed surface of asbestos fabric, is described. The aza-crown groups in these materials are bound with aqua complexes of H2SO4 or NaOH. The structure of the materials is examined, their adsorption characteristics are determined, and the rate of motion of H+ or OH- ions in electrochemical bridges is measured, while the formation of H2 and O2 in their cathodic and anodic polarization is determined as a function of voltage. It is shown that the upper layer of these materials is adsorption-active and electronand H+- or OH-- conductive, while the bottom layer is only H+- or OH-- conductive; through it, the upper layer is supplied with the H+ or OH- ions needed for the regeneration of the aqua complexes broken down to H2 and O2 on carbon particles.

  12. Monitoring Satellite-derived Surface Solar Radiation with Near Real Time Reference Data

    Science.gov (United States)

    Kim, H. Y.; Laszlo, I.; Liu, H.

    2015-12-01

    Geostationary satellite observations of the Earth are increasingly made more frequent. For example, Himawari-8 of Japanese Meteorological Agency takes images of the planet every 10 minutes in multiple bands. Similarly, the GOES-R satellite of the US National Oceanic and Atmospheric Administration (NOAA) will make observations every 5 to 15 minutes. Products, like shortwave (solar) radiation budget at the surface, derived from these observations have or will have similar rapid refresh rates. Routine, near-real time assessment of the quality of these products ideally requires the availability of near-real time reference data. Such near-real time data has recently become available from the NOAA Surface Radiation Budget Network (SURFRAD). These data are disseminated every 15 minutes. However, in contrast to non-real-time data with fully quality control, which have a latency of 24 hours or more, the near-real time data have less quality control applied to them in order to achieve low latency. To assess applicability of this near-real time SURFRAD data for the evaluation satellite products we are using them experimentally to evaluate the quality of Downward Shortwave Radiation at the surface (DSR) retrieved operationally every hour from GOES and made available in the Geostationary Surface and Insolation Product (GSIP) . Metrics (accuracy and precision) are computed to characterize the level of agreement between satellite retrievals and the near-real time reference data. These metrics are then compared with metrics from the evaluation with the non-real time, fully quality controlled reference. The comparison shows that monitoring of DSR with near-real time data is not very different from monitoring it with non-real time data and so DSR retrievals can be evaluated hourly or shorter times depending on reference data availability.

  13. Spatial heterogeneity of satellite derived land surface parameters and energy flux densities for LITFASS-area

    Directory of Open Access Journals (Sweden)

    A. Tittebrand

    2009-03-01

    Full Text Available Based on satellite data in different temporal and spatial resolution, the current use of frequency distribution functions (PDF for surface parameters and energy fluxes is one of the most promising ways to describe subgrid heterogeneity of a landscape. Objective of this study is to find typical distribution patterns of parameters (albedo, NDVI for the determination of the actual latent heat flux (L.E determined from highly resolved satellite data within pixel on coarser scale.

    Landsat ETM+, Terra MODIS and NOAA-AVHRR surface temperature and spectral reflectance were used to infer further surface parameters and radiant- and energy flux densities for LITFASS-area, a 20×20 km2 heterogeneous area in Eastern Germany, mainly characterised by the land use types forest, crop, grass and water. Based on the Penman-Monteith-approach L.E, as key quantity of the hydrological cycle, is determined for each sensor in the accordant spatial resolution with an improved parametrisation. However, using three sensors, significant discrepancies between the inferred parameters can cause flux distinctions resultant from differences of the sensor filter response functions or atmospheric correction methods. The approximation of MODIS- and AVHRR- derived surface parameters to the reference parameters of ETM (via regression lines and histogram stretching, respectively, further the use of accurate land use classifications (CORINE and a new Landsat-classification, and a consistent parametrisation for the three sensors were realized to obtain a uniform base for investigations of the spatial variability.

    The analyses for 4 scenes in 2002 and 2003 showed that for forest clear distribution-patterns for NDVI and albedo are found. Grass and crop distributions show higher variability and differ significantly to each other in NDVI but only marginal in albedo. Regarding NDVI-distribution functions NDVI was found to be the key variable for L.E-determination.

  14. Comparison of elevation and remote sensing derived products as auxiliary data for climate surface interpolation

    Science.gov (United States)

    Alvarez, Otto; Guo, Qinghua; Klinger, Robert C.; Li, Wenkai; Doherty, Paul

    2013-01-01

    Climate models may be limited in their inferential use if they cannot be locally validated or do not account for spatial uncertainty. Much of the focus has gone into determining which interpolation method is best suited for creating gridded climate surfaces, which often a covariate such as elevation (Digital Elevation Model, DEM) is used to improve the interpolation accuracy. One key area where little research has addressed is in determining which covariate best improves the accuracy in the interpolation. In this study, a comprehensive evaluation was carried out in determining which covariates were most suitable for interpolating climatic variables (e.g. precipitation, mean temperature, minimum temperature, and maximum temperature). We compiled data for each climate variable from 1950 to 1999 from approximately 500 weather stations across the Western United States (32° to 49° latitude and −124.7° to −112.9° longitude). In addition, we examined the uncertainty of the interpolated climate surface. Specifically, Thin Plate Spline (TPS) was used as the interpolation method since it is one of the most popular interpolation techniques to generate climate surfaces. We considered several covariates, including DEM, slope, distance to coast (Euclidean distance), aspect, solar potential, radar, and two Normalized Difference Vegetation Index (NDVI) products derived from Advanced Very High Resolution Radiometer (AVHRR) and Moderate Resolution Imaging Spectroradiometer (MODIS). A tenfold cross-validation was applied to determine the uncertainty of the interpolation based on each covariate. In general, the leading covariate for precipitation was radar, while DEM was the leading covariate for maximum, mean, and minimum temperatures. A comparison to other products such as PRISM and WorldClim showed strong agreement across large geographic areas but climate surfaces generated in this study (ClimSurf) had greater variability at high elevation regions, such as in the Sierra

  15. Assessment of the surface mass balance along the K-transect (Greenland ice sheet) from satellite-derived albedos

    NARCIS (Netherlands)

    Oerlemans, J.; Greuell, W.

    This paper explores the potential of using satellite-derived albedos to estimate the surface mass balance of the Kangerlussuaq transect (K-transect; Greenland ice sheet). We first retrieved surface albedos from Advanced Very High Resolution Radar data by using, among other techniques, a new

  16. Validation of AVHRR- and MODIS-derived albedos of snow and ice surfaces by means of helicopter measurements

    NARCIS (Netherlands)

    Greuell, W.; Oerlemans, J.

    2005-01-01

    We describe the validation of surface albedos of snow and glacier ice as derived from Advanced Very High Resolution Radiometer (AVHRR) and MOderate Resolution Imaging Spectrometer (MODIS) satellite data. For this purpose we measured surface albedos from a helicopter over Vatnajökull, Iceland, and

  17. Assessment of Satellite-Derived Surface Reflectances by NASA's CAR Airborne Radiometer over Railroad Valley, Nevada

    Science.gov (United States)

    Kharbouche, Said; Muller, Jan-Peter; Gatebe, Charles K.; Scanlon, Tracy; Banks, Andrew C.

    2017-01-01

    CAR (Cloud Absorption Radiometer) is a multi-angular and multi-spectral airborne radiometer instrument, whose radiometric and geometric characteristics are well calibrated and adjusted before and after each flight campaign. CAR was built by NASA (National Aeronautics and Space Administration) in 1984. On 16 May 2008, a CAR flight campaign took place over the well-known calibration and validation site of Railroad Valley in Nevada (38.504 deg N, 115.692 deg W).The campaign coincided with the overpasses of several key EO (Earth Observation) satellites such as Landsat-7, Envisat and Terra. Thus, there are nearly simultaneous measurements from these satellites and the CAR airborne sensor over the same calibration site. The CAR spectral bands are close to those of most EO satellites. CAR has the ability to cover the whole range of azimuth view angles and a variety of zenith angles depending on altitude and, as a consequence, the biases seen between satellite and CAR measurements due to both unmatched spectral bands and unmatched angles can be significantly reduced. A comparison is presented here between CARs land surface reflectance (BRF or Bidirectional Reflectance Factor) with those derived from Terra/MODIS (MOD09 and MAIAC), Terra/MISR, Envisat/MERIS and Landsat-7. In this study, we utilized CAR data from low altitude flights (approx. 180 m above the surface) in order to minimize the effects of the atmosphere on these measurements and then obtain a valuable ground-truth data set of surface reflectance. Furthermore, this study shows that differences between measurements caused by surface heterogeneity can be tolerated, thanks to the high homogeneity of the study site on the one hand, and on the other hand, to the spatial sampling and the large number of CAR samples. These results demonstrate that satellite BRF measurements over this site are in good agreement with CAR with variable biases across different spectral bands. This is most likely due to residual aerosol

  18. Delayed Ionization of Fullerenes and Fullerene Derivatives upon Laser Desorption and Surface Collision

    Science.gov (United States)

    Beck, R. D.; Weis, P.; Rockenberger, J.; Kappes, M. M.

    Delayed electron emission has been observed upon laser desorption for several fullerenes, endohedral metallofullerenes, and large carbon clusters formed by coalescence reactions. Odd-numbered carbon clusters and fullerene derivatives with exohedral functional groups do not show delayed ionization under similar conditions, presumably due to lower dissociation energies. Thus, delayed electron emission is suggested to be a characteristic indicator for strongly bound fullerene structures. Measurements of the rate of delayed electron emission are used together with structural information from other sources to calculate ionization potentials for these species. Selective observation of delayed electron emission from scattered {C}60* after surface impact and neutralization of {C}+{60 on graphite confirms an earlier report of this process by Whetten et al.6

  19. JVG9, a benzimidazole derivative, alters the surface and cytoskeleton of Trypanosoma cruzi bloodstream trypomastigotes.

    Science.gov (United States)

    Díaz-Chiguer, Dylan L; Hernández-Luis, Francisco; Nogueda-Torres, Benjamín; Castillo, Rafael; Reynoso-Ducoing, Olivia; Hernández-Campos, Alicia; Ambrosio, Javier R

    2014-09-01

    Trypanosoma cruzi has a particular cytoskeleton that consists of a subpellicular network of microtubules and actin microfilaments. Therefore, it is an excellent target for the development of new anti-parasitic drugs. Benzimidazole 2-carbamates, a class of well-known broad-spectrum anthelmintics, have been shown to inhibit the in vitro growth of many protozoa. Therefore, to find efficient anti-trypanosomal (trypanocidal) drugs, our group has designed and synthesised several benzimidazole derivatives. One, named JVG9 (5-chloro-1H-benzimidazole-2-thiol), has been found to be effective against T. cruzi bloodstream trypomastigotes under both in vitro and in vivo conditions. Here, we present the in vitro effects observed by laser scanning confocal and scanning electron microscopy on T. cruzi trypomastigotes. Changes in the surface and the distribution of the cytoskeletal proteins are consistent with the hypothesis that the trypanocidal activity of JVG9 involves the cytoskeleton as a target.

  20. JVG9, a benzimidazole derivative, alters the surface and cytoskeleton of Trypanosoma cruzi bloodstream trypomastigotes

    Directory of Open Access Journals (Sweden)

    Dylan L Díaz-Chiguer

    2014-09-01

    Full Text Available Trypanosoma cruzi has a particular cytoskeleton that consists of a subpellicular network of microtubules and actin microfilaments. Therefore, it is an excellent target for the development of new anti-parasitic drugs. Benzimidazole 2-carbamates, a class of well-known broad-spectrum anthelmintics, have been shown to inhibit the in vitro growth of many protozoa. Therefore, to find efficient anti-trypanosomal (trypanocidal drugs, our group has designed and synthesised several benzimidazole derivatives. One, named JVG9 (5-chloro-1H-benzimidazole-2-thiol, has been found to be effective against T. cruzi bloodstream trypomastigotes under both in vitro and in vivo conditions. Here, we present the in vitro effects observed by laser scanning confocal and scanning electron microscopy on T. cruzi trypomastigotes. Changes in the surface and the distribution of the cytoskeletal proteins are consistent with the hypothesis that the trypanocidal activity of JVG9 involves the cytoskeleton as a target.

  1. JVG9, a benzimidazole derivative, alters the surface and cytoskeleton of Trypanosoma cruzi bloodstream trypomastigotes

    Science.gov (United States)

    Díaz-Chiguer, Dylan L; Hernández-Luis, Francisco; Nogueda-Torres, Benjamín; Castillo, Rafael; Reynoso-Ducoing, Olivia; Hernández-Campos, Alicia; Ambrosio, Javier R

    2014-01-01

    Trypanosoma cruzi has a particular cytoskeleton that consists of a subpellicular network of microtubules and actin microfilaments. Therefore, it is an excellent target for the development of new anti-parasitic drugs. Benzimidazole 2-carbamates, a class of well-known broad-spectrum anthelmintics, have been shown to inhibit the in vitro growth of many protozoa. Therefore, to find efficient anti-trypanosomal (trypanocidal) drugs, our group has designed and synthesised several benzimidazole derivatives. One, named JVG9 (5-chloro-1H-benzimidazole-2-thiol), has been found to be effective against T. cruzi bloodstream trypomastigotes under both in vitro and in vivo conditions. Here, we present the in vitro effects observed by laser scanning confocal and scanning electron microscopy on T. cruzi trypomastigotes. Changes in the surface and the distribution of the cytoskeletal proteins are consistent with the hypothesis that the trypanocidal activity of JVG9 involves the cytoskeleton as a target. PMID:25317703

  2. Validating Satellite-Derived Land Surface Temperature with in Situ Measurements: A Public Health Perspective

    Science.gov (United States)

    Brines, Shannon J.; Brown, Daniel G.; Dvonch, J. Timothy; Gronlund, Carina J.; Zhang, Kai; Oswald, Evan M.; O’Neill, Marie S.

    2013-01-01

    Background: Land surface temperature (LST) and percent surface imperviousness (SI), both derived from satellite imagery, have been used to characterize the urban heat island effect, a phenomenon in which urban areas are warmer than non-urban areas. Objectives: We aimed to assess the correlations between LSTs and SI images with actual temperature readings from a ground-based network of outdoor monitors. Methods: We evaluated the relationships among a) LST calculated from a 2009 summertime satellite image of the Detroit metropolitan region, Michigan; b) SI from the 2006 National Land Cover Data Set; and c) ground-based temperature measurements monitored during the same time period at 19 residences throughout the Detroit metropolitan region. Associations between these ground-based temperatures and the average LSTs and SI at different radii around the point of the ground-based temperature measurement were evaluated at different time intervals. Spearman correlation coefficients and corresponding p-values were calculated. Results: Satellite-derived LST and SI values were significantly correlated with 24-hr average and August monthly average ground temperatures at all but two of the radii examined (100 m for LST and 0 m for SI). Correlations were also significant for temperatures measured between 0400 and 0500 hours for SI, except at 0 m, but not LST. Statistically significant correlations ranging from 0.49 to 0.91 were observed between LST and SI. Conclusions: Both SI and LST could be used to better understand spatial variation in heat exposures over longer time frames but are less useful for estimating shorter-term, actual temperature exposures, which can be useful for public health preparedness during extreme heat events. PMID:23777856

  3. Adsorption of cellulose derivatives on flat gold surfaces and on spherical gold particles.

    Science.gov (United States)

    Amirkhani, Masoud; Volden, Sondre; Zhu, Kaizheng; Glomm, Wilhelm R; Nyström, Bo

    2008-12-01

    The adsorption of hydroxyethylcellulose (HEC), ethyl(hydroxyethyl)cellulose (EHEC), and their hydrophobically modified counterparts HM-HEC and HM-EHEC has been studied on planar gold and citrate-covered gold surfaces by means of quartz crystal microbalance with dissipation monitoring (QCM-D), and on citrate-covered gold particles with the aid of dynamic light scattering (DLS). The QCM-D results indicate that larger amounts of polymer are adsorbed from aqueous solutions of HM-HEC and HM-EHEC on both substrates than from solutions of their unmodified analogues. The adsorption affinity for all the polymers, except EHEC, is higher on the citrate-covered surfaces than on the bare gold substrate. This indicates that more adsorption sites are activated in the presence of the citrate layer. The experimental adsorption data for all the polymers can be described fairly well by the Langmuir adsorption isotherm. However, at very low polymer concentrations significant deviations from the model are observed. The value of the hydrodynamic thickness of the adsorbed polymer layer (delta h), determined from DLS, rises with increasing polymer concentration for all the cellulose derivatives; a Langmuir type of isotherm can be used to roughly describe the adsorption behavior. Because of good solvent conditions for HEC the chains extend far out in the bulk at higher concentrations and the value of delta h is much higher than that of HM-HEC. The adsorption of EHEC and HM-EHEC onto gold particles discloses that the values of delta h are considerably higher for the hydrophobically modified cellulose derivative, and this finding is compatible with the trend in layer thickness estimated from the QCM-D measurements.

  4. Syntheses, spectral, electrochemical and thermal studies of mononuclear manganese(III) complexes with ligands derived from 1,2-propanediamine and 2-hydroxy-3 or 5-methoxybenzaldehyde: self-assembled monolayer formation on nanostructure zinc oxide thin film.

    Science.gov (United States)

    Habibi, Mohammad Hossein; Askari, Elham; Amirnasr, Mehdi; Amiri, Ahmad; Yamane, Yuki; Suzuki, Takayoshi

    2011-08-01

    Mononuclear Mn(III) complexes have been prepared via the Mn(II) reaction of an equimolar of Schiff-bases derived from reaction of 2-hydroxy-3-methoxybenzaldehyde or 2-hydroxy-5-methoxybenzaldehyde with 1,2-diaminopropane. Axial ligands L include: pyridine (py) and H(2)O. The resulting complexes have been characterized by FT-IR and UV-vis spectroscopy. The crystal structures of the complexes were determined and indicate that in the solid state the complex adopts a slightly distorted octahedral environment of the imine N and hydroxo O with the two axial ligands. The electrochemical reduction of these complexes at a glassy carbon electrode in acetonitrile solution indicates that the first reduction process corresponding to Mn(III)-Mn(II) is electrochemically quasi-reversible. Thermal stability of these complexes was determined by TG and DTG. Layers of these complexes were formed on nanostructure zinc oxide thin film and a red shift was observed when zinc oxide thin film is modified by complex. Copyright © 2011 Elsevier B.V. All rights reserved.

  5. Validation of Satellite-Derived Sea Surface Temperatures for Waters around Taiwan

    Directory of Open Access Journals (Sweden)

    Ming-An Lee

    2005-01-01

    Full Text Available In order to validate the Advanced Very High Resolution Radiometer (AVHRR-derived sea surface temperatures (SST of the waters around Taiwan, we generated a match-up data set of 961 pairs, which included in situ SSTs and concurrent AVHRR measurements for the period of 1998 to 2002. Availability of cloud-free images, i.e., images with more than 85% of cloud-free area in their coverage, was about 2.23% of all AVHRR images during the study period. The range of in situ SSTs was from _ to _ The satellite derived-SSTs through MCSST and NLSST algorithms were linearly related to the in situ SSTs with correlation coefficients of 0.985 and 0.98, respectively. The MCSSTs and NLSSTs had small biases of 0.009 _ and 0.256 _ with root mean square deviations of 0.64 _ and 0.801 _ respectively, therefore the AVHRR-based MCSSTs and NLSSTs had high accuracy in the seas around Taiwan.

  6. Holographic recording of surface relief gratings in stilbene azobenzene derivatives at 633 nm

    Energy Technology Data Exchange (ETDEWEB)

    Ozols, A; Saharov, D; Kokars, V; Kampars, V; Maleckis, A; Mezinskis, G; Pludons, A, E-mail: aozols@latnet.l [Faculty of Material Science and Applied Chemistry, Riga Technical University, Azenes iela 14/24, LV-1048, Riga (Latvia)

    2010-11-01

    Holographic recording in stilbene azobenzene derivatives by He-Ne 633 nm laser light has been experimentally studied. It was found that surface relief gratings (SRG) can be recorded by red light. Usually shorter wavelengths are used to induce the trans-cis photo-isomerization in organic materials. SRG with 2 {mu}m period and an amplitude of 130 nm have been recorded with 0.88 W/cm{sup 2} light in about 20 minutes in amorphous films of 3-(4-(bis(2-(trityloxy)ethyl)amino)phenyl)-2-(4-(2-bromo-4-nitrophenyl) diazenyl)phenyl)acrylonitrile spin-coated on glass substrates. Self-diffraction efficiency up to 17.4% and specific recording energy down to 114 J/(cm{sup 2}%) were measured. The recorded SRG were stable as proved by subsequent AFM measurements. The photo-induced changes in absorption spectra did not reveal noticeable signs of trans-cis transformations. Rather, spectrally uniform bleaching of the films took place. We conclude that a photothermally stimulated photo-destruction of chromophores is responsible for the SRG recording. The recording of stable SRG in the stilbene azobenzene derivatives we studied is accompanied by the recording of relaxing volume-phase gratings due to the photo-orientation of chromophores by the linearly polarized recording light. It should also be noted that holographic recording efficiency in stilbene azobenzene derivatives exhibit an unusual non-monotonic sample storage-time dependence presumably caused by the peculiarities of structural relaxation of the films.

  7. Influence of the surface quality due to a hole derived in initial material processing of cold sheets with drawing

    OpenAIRE

    Cvetkov, Slavco; Kocov, Atanas

    2010-01-01

    A research was performed about the influence of the surface quality due to a hole derived in initial material processing of cold-rolled steel sheets with drawing. This influence was researched through the surface quality obtained bu the type of preparation of the hole surface without prejudice to the precise measurement of the achieved quality (asperity). the aim is to indicate how the type of manufacturing the holes can improve the workability of cold-rolled sheets and help solve technical p...

  8. Surface and Electrochemical Studies on Silicon Diphosphide as Easy-to-Handle Anode Material for Lithium-Based Batteries-the Phosphorus Path.

    Science.gov (United States)

    Reinhold, Romy; Stoeck, Ulrich; Grafe, Hans-Joachim; Mikhailova, Daria; Jaumann, Tony; Oswald, Steffen; Kaskel, Stefan; Giebeler, Lars

    2018-02-28

    The electrochemical characteristics of silicon diphosphide (SiP 2 ) as a new anode material for future lithium-ion batteries (LIBs) are evaluated. The high theoretical capacity of about 3900 mA h g -1 (fully lithiated state: Li 15 Si 4 + Li 3 P) renders silicon diphosphide as a highly promising candidate to replace graphite (372 mA h g -1 ) as the standard anode to significantly increase the specific energy density of LIBs. The proposed mechanism of SiP 2 is divided into a conversion reaction of phosphorus species, followed by an alloying reaction forming lithium silicide phases. In this study, we focus on the conversion mechanism during cycling and report on the phase transitions of SiP 2 during lithiation and delithiation. By using ex situ analysis techniques such as X-ray powder diffraction, formed reaction products are identified. Magic angle spinning nuclear magnetic resonance spectroscopy is applied for the characterization of long-range ordered compounds, whereas X-ray photoelectron spectroscopy gives information of the surface-layer species at the interface of active material and electrolyte. Our SiP 2 anode material shows a high initial capacity of about 2700 mA h g -1 , whereas a fast capacity fading during the first few cycles occurs which is not necessarily expected. On the basis of our results, we conclude that besides other degradation effects, such as electrolyte decomposition and electrical contact loss, the rapid capacity fading originates from the formation of a low ion-conductive layer of LiP. This insulating layer hinders lithium-ion diffusion during lithiation and thereby mainly contributes to fast capacity fading.

  9. Construção de célula eletroquímica para observação de amostras in situ em estereomicroscópio Construction of an electrochemical cell to visualize samples in situ in stereomicroscope

    Directory of Open Access Journals (Sweden)

    Mônica Alessandra Silva Alencar

    2010-01-01

    Full Text Available The electrochemical study of glass like tungsten oxide derivatives requires the construction of special electrodes due to the fact that these glasses are not conductive. Electrodes modified with WO3 change their color when submitted to some potential perturbation. The color change of the electrochromic materials was observed in situ by coupling an electrochemical cell to a stereomicroscope. The constructed cell is versatile and may represent a great contribution to the electrochemical studies of materials, especially in the systems where it is interest to observe the working electrode surface during the electrochemical experiment.

  10. Surface mineral maps of Afghanistan derived from HyMap imaging spectrometer data, version 2

    Science.gov (United States)

    Kokaly, Raymond F.; King, Trude V.V.; Hoefen, Todd M.

    2013-01-01

    This report presents a new version of surface mineral maps derived from HyMap imaging spectrometer data collected over Afghanistan in the fall of 2007. This report also describes the processing steps applied to the imaging spectrometer data. The 218 individual flight lines composing the Afghanistan dataset, covering more than 438,000 square kilometers, were georeferenced to a mosaic of orthorectified Landsat images. The HyMap data were converted from radiance to reflectance using a radiative transfer program in combination with ground-calibration sites and a network of cross-cutting calibration flight lines. The U.S. Geological Survey Material Identification and Characterization Algorithm (MICA) was used to generate two thematic maps of surface minerals: a map of iron-bearing minerals and other materials, which have their primary absorption features at the shorter wavelengths of the reflected solar wavelength range, and a map of carbonates, phyllosilicates, sulfates, altered minerals, and other materials, which have their primary absorption features at the longer wavelengths of the reflected solar wavelength range. In contrast to the original version, version 2 of these maps is provided at full resolution of 23-meter pixel size. The thematic maps, MICA summary images, and the material fit and depth images are distributed in digital files linked to this report, in a format readable by remote sensing software and Geographic Information Systems (GIS). The digital files can be downloaded from http://pubs.usgs.gov/ds/787/downloads/.

  11. Electrochemical Science and Technology

    CERN Document Server

    Oldham, Keith; Bond, Alan

    2011-01-01

    The book addresses the scientific principles underlying electrochemistry. Starting with the basic concepts of electricity, the early chapters discuss the physics and chemistry of the materials from which electrochemical cells are constructed and the properties that make these materials appropriate as cell components. Much of the importance of electrochemistry lies in the conversion of electrical energy into chemical energy and vice versa; the thermodynamics of these processes is described, in the context of a wide range of applications of these interconversions. An electrode is a surface at wh

  12. Surface radiation at sea validation of satellite-derived data with shipboard measurements

    Directory of Open Access Journals (Sweden)

    Hein Dieter Behr

    2009-03-01

    Full Text Available Quality-controlled and validated radiation products are the basis for their ability to serve the climate and solar energy community. Satellite-derived radiation fluxes are well preferred for this task as they cover the whole research area in time and space. In order to monitor the accuracy of these data, validation with well maintained and calibrated ground based measurements is necessary. Over sea, however, long-term accurate reference data sets from calibrated instruments recording radiation are scarce. Therefore data from research vessels operating at sea are used to perform a reasonable validation. A prerequisite is that the instruments on board are maintained as well as land borne stations. This paper focuses on the comparison of radiation data recorded on board of the German Research Vessel "Meteor" during her 13 months cruise across the Mediterranean and the Black Sea with CM-SAF products using NOAA- and MSG-data (August 2006-August 2007: surface incoming short-wave radiation (SIS and surface downward long-wave radiation (SDL. Measuring radiation fluxes at sea causes inevitable errors, e.g.shadowing of fields of view of the radiometers by parts of the ship. These ship-inherent difficulties are discussed at first. A comparison of pairs of ship-recorded and satellite-derived mean fluxes for the complete measuring period delivers a good agreement: the mean bias deviation (MBD for SIS daily means is −7.6 W/m2 with a median bias of −4 W/m2 and consistently the MBD for monthly means is −7.3 W/m2, for SDL daily means the MBD is 8.1 and 6 W/m2 median bias respectively. The MBD for monthly means is 8.2 W/m2. The variances of the daily means (ship and satellite have the same annual courses for both fluxes. No significant dependence of the bias on the total cloud cover recorded according to WMO (1969 has been found. The results of the comparison between ship-based observations and satellite retrieved surface radiation reveal the good accuracy

  13. A quadruplet electrochemical platform for ultrasensitive and simultaneous detection of ascorbic acid, dopamine, uric acid and acetaminophen based on a ferrocene derivative functional Au NPs/carbon dots nanocomposite and graphene

    Energy Technology Data Exchange (ETDEWEB)

    Yang, Liuqing; Huang, Na; Lu, Qiujun; Liu, Meiling, E-mail: liumeilingww@126.com; Li, Haitao; Zhang, Youyu; Yao, Shouzhuo

    2016-01-15

    In this work, a new nanomaterial of thiol functional ferrocene derivative (Fc-SH) stabilized Au NPs/carbon dots nanocomposite (Au/C NC) coupling with graphene modified glassy carbon electrode (Fc-S-Au/C NC/graphene/GCE) was fabricated to serve as a quadruplet detection platform for ultrasensitive and simultaneous determination of ascorbic acid (AA), dopamine (DA), uric acid (UA) and acetaminophen (AC). The Au/C NC was synthesized by adding HAuCl{sub 4} into carbon nanodots solution without using any additional reductant and stabilizing agent. Then the Fc-SH was utilized as the protective and capping agent to modify the Au/C NC. Transmission electron microscopy (TEM), UV–Vis, Fourier-transform infrared (FT-IR), scanning electron microscopy (SEM), cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS) were adopted to characterize the morphology and electrochemical properties of the materials and the electrodes. The Fc-S-Au/C NC/graphene/GCE exhibits a synergistic catalytic and amplification effects towards oxidation of AA, DA, UA and AC owing to the existence of the nanomaterial and electron mediator. When simultaneous detection of AA, DA, UA and AC, the oxidation peak potentials of the four compounds on the electrode can be well separated and the peak currents were linearly dependent on their concentrations. The quadruplet detection platform shows excellent linear range and ultrasensitive response to the four components, the detection limits were estimated to be as low as 1.00, 0.05, 0.12 and 0.10 μM (S/N = 3), and the modified electrode exhibits excellent stability and reproducibility. The proposed electrode has been successfully applied to detect of these four analytes in real samples with satisfactory results. - Highlights: • A quadruplet detection platform for ultrasensitive and simultaneous determination of AA, DA, UA and AC was constructed. • The platform was based on the composite containing Au/C NC, graphene and a ferrocene

  14. Derivation of surface temperature from current and future satellite: Focus on land

    Science.gov (United States)

    Sun, Donglian

    . Analysis of the directional viewing effect shows that with increased number of window channels, the LST accuracy is improved. The four-channel algorithm proposed for the MSG/SEVIRI or ADEOS/GLI is an improvement over the proposed split window and the three-channel LST algorithms for GOES-8, GOES-10 and NOAA/AVHRR imagers. Evaluation against observations from the atmospheric radiation measurement program (ARM) and observations from the surface radiation budget network (SURFARD) shows that LST can be determined from real-time GOES-8 observations within accuracy of about 1--2 K in root mean square (RMS) error and precision of about 1 K, with less than 1 K bias. The likelihood of deriving LST under cloudy conditions from satellite infrared measurements is evaluated. A look-up table approach is developed to correct the brightness temperature under partially cloudy conditions. For all kind of cloudy conditions, two approaches are explored: clear neighbor correction with numerical model prediction and surface solar radiation; and air temperature adjustment. The LST RMS error from the clear neighbor algorithm under cloudy condition is 1--2 K. An air temperature adjustment scheme can generate LST with a RMS error of 2--3 K. These results indicate that under cloudy conditions, the error from the clear neighbor algorithm is smaller than that from microwave retrievals and the retrieval is possible at higher spatial resolution. (Abstract shortened by UMI.)

  15. Nanomaterial-Based Electrochemical Immunosensors for Clinically Significant Biomarkers

    National Research Council Canada - National Science Library

    Niina J Ronkainen; Stanley L Okon

    2014-01-01

    .... In general, nanomaterials-based electrochemical immunosensors amplify the sensitivity by facilitating greater loading of the larger sensing surface with biorecognition molecules as well as improving...

  16. Multi-layer seal for electrochemical devices

    Science.gov (United States)

    Chou, Yeong-Shyung [Richland, WA; Meinhardt, Kerry D [Kennewick, WA; Stevenson, Jeffry W [Richland, WA

    2010-09-14

    Multi-layer seals are provided that find advantageous use for reducing leakage of gases between adjacent components of electrochemical devices. Multi-layer seals of the invention include a gasket body defining first and second opposing surfaces and a compliant interlayer positioned adjacent each of the first and second surfaces. Also provided are methods for making and using the multi-layer seals, and electrochemical devices including said seals.

  17. SIRPA is a specific cell-surface marker for isolating cardiomyocytes derived from human pluripotent stem cells

    OpenAIRE

    Dubois, Nicole C.; Craft, April M; Sharma, Parveen; Elliott, David A.; Stanley, Edouard G.; Elefanty, Andrew G.; Gramolini, Anthony; Keller, Gordon

    2011-01-01

    To identify cell-surface markers specific to human cardiomyocytes, we screened cardiovascular cell populations derived from human embryonic stem cells (hESCs) against a panel of 370 known CD antibodies. This screen identified the signal-regulatory protein alpha (SIRPA) as a marker expressed specifically on cardiomyocytes derived from hESCs and human induced pluripotent stem cells (hiPSCs), and PECAM, THY1, PDGFRB and ITGA1 as markers of the nonmyocyte population. Cell sorting with an antibody...

  18. Surface Activity Distributions of Comet 67P/Churyumov-Gerasimenko Derived from VIRTIS Images

    Science.gov (United States)

    Fougere, Nicolas; Combi, Michael R.; Tenishev, Valeriy; Migliorini, Alessandra; Bockelee-Morvan, Dominique; Fink, Uwe; Filacchione, Gianrico; Rinaldi, Giovanna; Capaccioni, Fabrizio; Toth, Gabor; Gombosi, T. I.; Hansen, Kenneth C.; Huang, Zhenguang; Shou, Yinsi; VIRTIS Team

    2017-10-01

    The outgassing mechanism of comets still remains a critical question to better understand these objects. The Rosetta mission gave some insight regarding the potential activity distribution from the surface of the nucleus of comet 67P/Churyumov-Gerasimenko, Fougere et al. (2016, Astronomy & Astrophysics, Volume 588, id.A134, 11 pp and Monthly Notices of the Royal Astronomical Society, Volume 462, Issue Suppl_1, p.S156-S169) used a spherical harmonics inversion scheme with in-situ measurements from the ROSINA instrument to derive mapping of the broad distribution of potential activity at the surface of the nucleus. Marschall et al. (2016, Astronomy & Astrophysics, doi: 10.1051/0004-6361/201730849) based on the appearance of dust active areas suggested that the so-called “neck” region and regions with fractured cliffs and locally steep slopes show more activity than the rest of comet 67P’s nucleus. Using in situ ROSINA measurements from a distance makes it difficult to distinguish between these two scenarios because the fast expansion of the gas and large molecular mean free paths prevents distinguishing small outgassing features even when the spacecraft was in bound orbits within 10 km from the nucleus. In this paper, we present a similar numerical inversion approach using VIRTIS images, which should better probe the very inner coma of comet 67P and give more detailed information about the outgassing activity. Support from contracts JPL #1266314 and #1266313 from the US Rosetta Project and grant NNX14AG84G from the NASA Planetary Atmospheres Program are gratefully acknowledged.

  19. Deriving Algorithms for the Remote Sensing of Carbon Dioxide Fugacity at the Ocean Surface

    Science.gov (United States)

    Minnett, P. J.; Wickramaratna, K.; Kubat, M.

    2010-12-01

    As concentrations of carbon dioxide in the atmosphere continue to rise, the capacity of the ocean to act as a carbon dioxide sink is of critical importance as it is the major sink of anthropogenic carbon dioxide. Uncertainties in our ability to quantify the role of the oceans in the carbon cycle, especially in computing the gas fluxes between atmosphere and ocean on global scales, leads directly to uncertainty in predicting the response of the of the climate system to increasing levels of carbon dioxide in the atmosphere. Here we report on a study to improve the accuracy of the retrievals of surface fugacity from earth observation satellites. A large data set of in situ measurements from equipment on the Royal Caribbean Cruise Lines ship Explorer of the Seas in the Caribbean Sea and western tropical Atlantic Ocean the relationship between the carbon dioxide concentration and variables measurable from space is explored using advanced computational techniques to improve on prior results derived by linear regression. Using natural selection as a conceptual model, the Genetic Algorithm approach maintains a population of “tentative” solutions that are subjected to “survival of the fittest” tests and to operators that implement mutation and recombination (mutual exchange of the “genetic information”). In our implementation, each specimen in the population represents one formula, expressed by a tree-like data structure. The fitness function that quantifies the individual's survival chances is defined as the mean square error scored by the given formula on the training data. We demonstrate in this case study that not only can the accuracy of satellite retrievals of surface fugacity of carbon dioxide be improved by using algorithms based on the information content of the data sets, but also the regions in which individual algorithms are applicable can also be determined. These regions align with the underlying dynamical oceanographic features. This approach can

  20. Influence of Light Emitting Diode-Derived Blue Light Overexposure on Mouse Ocular Surface.

    Science.gov (United States)

    Lee, Hyo Seok; Cui, Lian; Li, Ying; Choi, Ji Suk; Choi, Joo-Hee; Li, Zhengri; Kim, Ga Eon; Choi, Won; Yoon, Kyung Chul

    2016-01-01

    To investigate the influence of overexposure to light emitting diode (LED)-derived light with various wavelengths on mouse ocular surface. LEDs with various wavelengths were used to irradiate C57BL/6 mice at an energy dose of 50 J/cm2, twice a day, for 10 consecutive days. The red, green, and blue groups represented wavelengths of 630 nm, 525 nm, and 410 nm, respectively. The untouched group (UT) was not exposed to LED light and served as the untreated control. Tear volume, tear film break-up time (TBUT), and corneal fluorescein staining scores were measured on days 1, 3, 5, 7, and 10. Levels of interferon (IFN)-γ, interleukin (IL)-1β, IL-6, and tumor necrosis factor (TNF)-α were measured in the cornea and conjunctiva using a multiplex immunobead assay at day 10. Levels of malondialdehyde (MDA) were measured with an enzyme-linked immunosorbent assay. Flow cytometry, 2'7'-dichlorofluorescein diacetate (DCF-DA) assay, histologic analysis, immunohistochemistry with 4-hydroxynonenal, and terminal deoxynucleotidyl transferase-mediated dUTP-nick end labeling (TUNEL) staining were also performed. TBUT of the blue group showed significant decreases at days 7 and 10, compared with the UT and red groups. Corneal fluorescein staining scores significantly increased in the blue group when compared with UT, red, and green groups at days 5, 7, and 10. A significant increase in the corneal levels of IL-1β and IL-6 was observed in the blue group, compared with the other groups. The blue group showed significantly increased reactive oxygen species production in the DCF-DA assay and increased inflammatory T cells in the flow cytometry. A significantly increased TUNEL positive cells was identified in the blue group. Overexposure to blue light with short wavelengths can induce oxidative damage and apoptosis to the cornea, which may manifest as increased ocular surface inflammation and resultant dry eye.

  1. Surface Solar Radiation in North America: Observations, Reanalyses, Satellite and Derived Products

    Science.gov (United States)

    Slater, A. G.

    2015-12-01

    Observations of daily surface solar/shortwave radiation data from over 4000 stations have been gathered, covering much of the lower 48 continental states of the US as well as portions of Alberta and British Columbia, Canada. The quantity of data increases almost linearly from 1998 when only several hundred stations had data. A quality control procedure utilizing threshold values along with computing the clear sky radiation envelope for individual stations was implemented to both screen bad data and rescue informative data. Over two thirds of the observations are seen as acceptable. Fifteen different surface solar radiation products are assessed relative to observations, including reanalyses (20thC, CFSRR, ERAI, JRA-55, MERRA, NARR, NCEP), derived products (CRU_NCEP, DAYMET, GLDAS, GSWP3, MsTMIP, NLDAS) and two satellite products (CERES and GOES). All except the CERES product are daily or finer in temporal resolution. The root mean square error of spatial biases is greater than 18Wm-2 for 13 of the 15 products over the summer season (June, July, August). None of the daily resolution products fulfill all three desirable criteria of low (bias, high correlation with observed cloudiness and correct distribution of clear sky radiation. Some products display vestiges of underlying algorithm issues (e.g. from MTCLIM ver4.3) or bias correction methods. A new bias correction method is introduced that preserves clear sky radiation values and better replicates cloudiness statistics. The current quantity of data over the continental US suggests a solar radiation product based on, or enhanced with, observations is feasible.

  2. Influence of Light Emitting Diode-Derived Blue Light Overexposure on Mouse Ocular Surface.

    Directory of Open Access Journals (Sweden)

    Hyo Seok Lee

    Full Text Available To investigate the influence of overexposure to light emitting diode (LED-derived light with various wavelengths on mouse ocular surface.LEDs with various wavelengths were used to irradiate C57BL/6 mice at an energy dose of 50 J/cm2, twice a day, for 10 consecutive days. The red, green, and blue groups represented wavelengths of 630 nm, 525 nm, and 410 nm, respectively. The untouched group (UT was not exposed to LED light and served as the untreated control. Tear volume, tear film break-up time (TBUT, and corneal fluorescein staining scores were measured on days 1, 3, 5, 7, and 10. Levels of interferon (IFN-γ, interleukin (IL-1β, IL-6, and tumor necrosis factor (TNF-α were measured in the cornea and conjunctiva using a multiplex immunobead assay at day 10. Levels of malondialdehyde (MDA were measured with an enzyme-linked immunosorbent assay. Flow cytometry, 2'7'-dichlorofluorescein diacetate (DCF-DA assay, histologic analysis, immunohistochemistry with 4-hydroxynonenal, and terminal deoxynucleotidyl transferase-mediated dUTP-nick end labeling (TUNEL staining were also performed.TBUT of the blue group showed significant decreases at days 7 and 10, compared with the UT and red groups. Corneal fluorescein staining scores significantly increased in the blue group when compared with UT, red, and green groups at days 5, 7, and 10. A significant increase in the corneal levels of IL-1β and IL-6 was observed in the blue group, compared with the other groups. The blue group showed significantly increased reactive oxygen species production in the DCF-DA assay and increased inflammatory T cells in the flow cytometry. A significantly increased TUNEL positive cells was identified in the blue group.Overexposure to blue light with short wavelengths can induce oxidative damage and apoptosis to the cornea, which may manifest as increased ocular surface inflammation and resultant dry eye.

  3. Surface-enhanced Raman scattering studies on the interaction of phosphonate derivatives of imidazole, thiazole, and pyridine with a silver electrode in aqueous solution.

    Science.gov (United States)

    Podstawka, Edyta; Kudelski, Andrzej; Olszewski, Tomasz K; Boduszek, Bogdan

    2009-07-23

    Surface-enhanced Raman scattering (SERS) spectra from phosphonate derivatives of N-heterocyclic aromatic compounds immobilized on an electrochemically roughened silver electrode surface are reported and compared to Raman spectra of the corresponding solid species. The tested compounds contain imidazole [ImMeP ([hydroxy-(1H-imidazol-5-yl)-methyl]-phosphonic acid) and (ImMe)2P (bis[hydroxy-(1H-imidazol-4-yl)-methyl]-phosphinic acid)]; thiazole [BAThMeP ((butylamino-thiazol-2-yl-methyl)-phosphonic acid) and BzAThMeP ((benzylamino-thiazol-2-yl-methyl)-phosphonic acid)]; and pyridine ((PyMe)2P (bis[(hydroxy-pyridin-3-yl-methyl)]-phosphinic acid) aromatic rings. Changes in wavenumber, broadness, and the enhancement of N-heterocyclic aromatic ring bands upon adsorption are consistent with the adsorption primarily occurring through the N lone pair of electrons with the ring arranged in a largely edge-on manner for ImMeP and BzAThMeP or in a slightly inclined orientation to the silver electrode surface at an intermediate angle from the surface normal for (ImMe)2P, BAThMeP, and (PyMe)2P. A strong enhancement of a roughly 1500 cm(-1) SERS signal for ImMeP and (PyMe)2P is also observed. This phenomenon is attributed to the formation of a localized C=C bond, which is accompanied by a decrease in the ring-surface pi-electrons' overlap. In addition, more intense SERS bands due to the benzene ring in BzAThMeP are observed than those observed for the thiazole ring, which suggests a preferential adsorption of benzene. Some interaction of a phosphonate unit is also suggested but with moderate strength between biomolecules. The strength of the P=O coordination to the silver electrode is highest for ImMeP but lowest for BzAThMeP. For all studied biomolecules, the contribution of the structural components to their ability to interact with their receptors was correlated with the SERS patterns.

  4. Fetoprotein Derived Short Peptide Coated Nanostructured Amphiphilic Surfaces for Targeting Mouse Breast Cancer Cells

    Science.gov (United States)

    Brown, Alexandra M.; Miranda-Alarćon, Yoliem S.; Knoll, Grant A.; Santora, Anthony M.; Banerjee, Ipsita A.

    In this work, self-assembled tumor targeting nanostructured surfaces were developed from a newly designed amphiphile by conjugating boc protected isoleucine with 2,2‧ ethylenedioxy bis ethylamine (IED). To target mouse mammary tumor cells, a short peptide sequence derived from the human alpha-fetoprotein (AFP), LSEDKLLACGEG was attached to the self-assembled nanostructures. Tumor targeting and cell proliferation were examined in the presence of nanoscale assemblies. To further obliterate mouse breast tumor cells, the chemotherapeutic drug tamoxifen was then entrapped into the nanoassemblies. Our studies indicated that the targeting systems were able to efficiently encapsulate and release tamoxifen. Cell proliferation studies showed that IED-AFP peptide loaded with tamoxifen decreased the proliferation of breast cancer cells while in the presence of the IED-AFP peptide nanoassemblies alone, the growth was relatively slower. In the presence of human dermal fibroblasts however cell proliferation continued similar to controls. Furthermore, the nanoscale assemblies were found to induce apoptosis in mouse breast cancer cells. To examine live binding interactions, SPR analysis revealed that tamoxifen encapsulated IED-AFP peptide nanoassemblies bound to the breast cancer cells more efficiently compared to unencapsulated assemblies. Thus, we have developed nanoscale assemblies that can specifically bind to and target tumor cells, with increased toxicity in the presence of a chemotherapeutic drug.

  5. In-vitro cell adhesion and proliferation of adipose derived stem cell on hydroxyapatite composite surfaces.

    Science.gov (United States)

    Pulyala, Praneetha; Singh, Akshay; Dias-Netipanyj, Marcela Ferreira; Cogo, Sheron Compos; Santos, Luciane S; Soares, Paulo; Gopal, Vasanth; Suganthan, V; Manivasagam, Geetha; Popat, Ketul C

    2017-06-01

    The goal of this work was to enhance the mechanical strength and fracture toughness of brittle hydroxyapatite (HAP) by reinforcing it with nanocomposites such as graphene oxide (GO), carbon nanotubes (CNT) and Titania. The goal was also to evaluate the cytotoxicity and the cellular adhesion/proliferation of these composites. The composites were characterized for their crystallinity, functionality, morphology and mechanical properties. Altering the composition by adding 1wt% GO and CNT significantly altered the wettability, hardness and roughness. Further, X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FITR) and X-ray photoelectron spectroscopy (XPS) results confirm the crystal structure, bulk chemical composition and surface elemental composition respectively of the composites. The bulk hardness of HAP with CNT was significantly higher than that of HAP. The wettability of HAP with GO was significantly lower than that of HAP with GO and Titania. Adipose Derived Stem Cells (ADSCs) were used for this study to evaluate cytotoxicity and viability. HAP with CNT and HAP with CNT and Titania were found to be least cytotoxic compared to other composites as evaluated by Lactate Dehydrogenase (LDH) assay and alamarBlue assay. ADSC adhesion and proliferation was investigated after 1, 4 and 7days of culture using fluorescence microscopy. All the composites nurtured ADSC adhesion and proliferation, however, distinct morphological changes were observed by using Scanning Electron Microscopy (SEM). Overall, these composites have the potential to be used as bone graft substitutes. Copyright © 2017 Elsevier B.V. All rights reserved.

  6. Labile Zn ions on octacalcium phosphate-derived Zn-containing hydroxyapatite surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Honda, Yoshitomo; Anada, Takahisa; Morimoto, Shinji [Division of Craniofacial Function Engineering (CFE), Tohoku University Graduate School of Dentistry, Sendai (Japan); Suzuki, Osamu, E-mail: suzuki-o@m.tohoku.ac.jp [Division of Craniofacial Function Engineering (CFE), Tohoku University Graduate School of Dentistry, Sendai (Japan)

    2013-05-15

    We previously synthesized and characterized zinc-containing octacalcium phosphate (OCP) and its hydrolyzed Ca-deficient hydroxyapatite (HA). In the present report, we attempted to define the state of Zn in the OCP-derived Zn-calcium phosphates (CaPs) in relation to the presence of specific amino acids. Zn-containing OCPs were prepared in solutions that included Zn ions up to a concentration of 3.5 mM, and their hydrolyzates [hydrolyzed (hy)-Zn-CaP] were obtained in hot water. The materials were characterized by x-ray diffraction and scanning electron microscopy. The concentration of Ca and Zn ions at room temperature was determined by analyzing the supernatant after incubating the materials in α-minimal essential medium (α-MEM) and HEPES buffer including cysteine, histidine, lysine, aspartic acid, and glutamic acid. Zn ions were more dissolved in α-MEM than HEPES buffer in the absence of amino acids. The inclusion of the amino acids enhanced Zn dissolution by several hundred fold, even in HEPES buffer. Among the amino acids, both cysteine and histidine enhanced the release of Zn. The effect was particularly remarkable with cysteine even in the presence of the other amino acids tested. These results indicate that Zn ions are present as a surface labile pool, which tends to be preferentially desorbed by cysteine, a ubiquitous molecule present in serum.

  7. Estimating Biomass of Barley Using Crop Surface Models (CSMs Derived from UAV-Based RGB Imaging

    Directory of Open Access Journals (Sweden)

    Juliane Bendig

    2014-10-01

    Full Text Available Crop monitoring is important in precision agriculture. Estimating above-ground biomass helps to monitor crop vitality and to predict yield. In this study, we estimated fresh and dry biomass on a summer barley test site with 18 cultivars and two nitrogen (N-treatments using the plant height (PH from crop surface models (CSMs. The super-high resolution, multi-temporal (1 cm/pixel CSMs were derived from red, green, blue (RGB images captured from a small unmanned aerial vehicle (UAV. Comparison with PH reference measurements yielded an R2 of 0.92. The test site with different cultivars and treatments was monitored during “Biologische Bundesanstalt, Bundessortenamt und CHemische Industrie” (BBCH Stages 24–89. A high correlation was found between PH from CSMs and fresh biomass (R2 = 0.81 and dry biomass (R2 = 0.82. Five models for above-ground fresh and dry biomass estimation were tested by cross-validation. Modelling biomass between different N-treatments for fresh biomass produced the best results (R2 = 0.71. The main limitation was the influence of lodging cultivars in the later growth stages, producing irregular plant heights. The method has potential for future application by non-professionals, i.e., farmers.

  8. REMOTE SENSING AND SURFACE ENERGY FLUX MODELS TO DERIVE EVAPOTRANSPIRATION AND CROP COEFFICIENT

    Directory of Open Access Journals (Sweden)

    Salvatore Barbagallo

    2008-06-01

    Full Text Available Remote sensing techniques using high resolution satellite images provide opportunities to evaluate daily crop water use and its spatial and temporal distribution on a field by field basis. Mapping this indicator with pixels of few meters of size on extend areas allows to characterize different processes and parameters. Satellite data on vegetation reflectance, integrated with in field measurements of canopy coverage features and the monitoring of energy fluxes through the soil-plant-atmosphere system, allow to estimate conventional irrigation components (ET, Kc thus improving irrigation strategies. In the study, satellite potential evapotranspiration (ETp and crop coefficient (Kc maps of orange orchards are derived using semi-empirical approaches between reflectance data from IKONOS imagery and ground measurements of vegetation features. The monitoring of energy fluxes through the orchard allows to estimate actual crop evapotranspiration (ETa using energy balance and the Surface Renewal theory. The approach indicates substantial promise as an efficient, accurate and relatively inexpensive procedure to predict actual ET fluxes and Kc from irrigated lands.

  9. Surface morphology and nanomechanical properties of tribological antiwear films derived from zinc dialkyl dithiophosphate compounds

    Science.gov (United States)

    Aktary, Mirwais

    The protection of mechanical equipment from wear is of significant economic interest. It has been estimated that up to half of a percent of the gross domestic product of industrialized countries goes to replacing mechanical components that have lost compliance due to wear. Antiwear additives are key ingredients in lubrication oils that assist in protecting components from wear during high loads. These agents form sacrificial films on metal parts that limit the adhesion between the contacting surfaces and reduce the wear rate considerably. One of the most common classes of compounds employed as an antiwear agent is zinc dialkyldithiophosphates (ZDDP). This work will explore the formation, structure, and mechanical properties of ZDDP derived antiwear films on the nanoscale. These studies are important because the macroscopic performance of antiwear coatings is dictated by their nanoscale surface properties. As a first study, scanning force microscopy (SFM) is employed to track the formation of films formed from the thermooxidative decomposition of ZDDP on gold substrates. The SFM analysis is correlated with infrared spectroscopy to relate surface structure to chemical composition. The morphology and mechanical strength of ZDDP tribofilms formed at the interface of sliding stainless steel contacts is also investigated. The tribofilms evolve morphologically with contact time and are characterized by distinct segregated islands at low times that transforms to a full film at longer times. The nanomechanical properties of the tribofilms are evaluated by nanoindentation analysis. It is found that the films are mechanically softer than the underlying steel substrate. SFM and nanoindentation analyses reveal that calcium sulphonate detergents promote the formation of ZDDP tribofilms and impart to them greater mechanical stability. By contrast succinimide dispersants reduce the capacity of ZDDP to form effective antiwear films. The first application of SFM and nanoindentation

  10. SAFARI 2000 AVHRR-derived Land Surface Temperature Maps, Africa, 1995-2000

    Data.gov (United States)

    National Aeronautics and Space Administration — Land Surface Temperature (LST) is a key indicator of land surface states, and can provide information on surface-atmosphere heat and mass fluxes, vegetation water...

  11. SAFARI 2000 AVHRR-derived Land Surface Temperature Maps, Africa, 1995-2000

    Data.gov (United States)

    National Aeronautics and Space Administration — ABSTRACT: Land Surface Temperature (LST) is a key indicator of land surface states, and can provide information on surface-atmosphere heat and mass fluxes,...

  12. Advective surface velocity in the north west Pacific derived from NOAA AVHRR images

    Digital Repository Service at National Institute of Oceanography (India)

    Pankajakshan, T.; Akiyama, M.; Okada, Y.; Sugimori, Y.

    Using sequential AVHRR images in November 1983, nearsurface advective velocities are derived in the region Kuroshio south of Japan. For deriving the velocities two methods are used. One is the Method of Cross Correlation (MCC), using image pair...

  13. Morphology controlled synthesis of platinum nanoparticles performed on the surface of graphene oxide using a gas-liquid interfacial reaction and its application for high-performance electrochemical sensing.

    Science.gov (United States)

    Bai, Wushuang; Sheng, Qinglin; Zheng, Jianbin

    2016-07-21

    In this paper, we report a novel morphology-controlled synthetic method. Platinum (Pt) nanoparticles with three kinds of morphology (aggregation-like, cube-like and globular) were grown on the surface of graphene oxide (GO) using a simple gas-liquid interfacial reaction and Pt/GO nanocomposites were obtained successfully. According to the experimental results, the morphology of the Pt nanoparticles can be controlled by adjusting the reaction temperature with the protection of chitosan. The obtained Pt/GO nanocomposites were characterized using transmission electron microscopy (TEM), X-ray diffraction (XRD) and fourier transform infrared spectroscopy (FTIR). Then the Pt/GO nanocomposites with the three kinds of morphology were all used to fabricate electrochemical sensors. The electrochemical experimental results indicated that compared with various reported electrochemical sensors, the Pt/GO modified sensors in this work exhibit a low detection limit, high sensitivity and an extra wide linear range for the detection of nitrite. In addition, the synthesis of Pt particles based on a gas-liquid interfacial reaction provides a new platform for the controllable synthesis of nanomaterials.

  14. Influence of ionic liquid on pseudocapacitance performance of electrochemically synthesized conductive polymer: Electrochemical and theoretical investigation.

    Science.gov (United States)

    Ehsani, A; Kowsari, E; Dashti Najafi, M; Safari, R; Mohammad Shiri, H

    2017-08-15

    This study demonstrates a method for improving supercapacitive performance of electrochemically synthesized conductive polymer. In this regards, 1-Butyl-3-methyl imidazolium hexafluorophosphate (BI) as a new high efficient ionic liquid was synthesized using chemical approach and then fabricated POAP/BI films by electro-polymerization of POAP in the presence of BI to serve as the active electrode for electrochemical supercapacitor. Theoretical study (AIM) and electrochemical analysis have been used for characterization of ionic liquid and POAP/BI composite film. Different electrochemical methods including galvanostatic charge-discharge experiments, cyclic voltammetry and electrochemical impedance spectroscopy are carried out in order to investigate the performance of the system. This work introduces new most efficient materials for electrochemical redox capacitors with advantages including ease synthesis, high active surface area and stability in an aqueous electrolyte. Copyright © 2017 Elsevier Inc. All rights reserved.

  15. Computer-assisted electrochemical fabrication of a highly selective and sensitive amperometric nitrite sensor based on surface decoration of electrochemically reduced graphene oxide nanosheets with CoNi bimetallic alloy nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Gholivand, Mohammad-Bagher, E-mail: mbgholivand2013@gmail.com [Faculty of Chemistry, Razi University, Kermanshah 671496734 (Iran, Islamic Republic of); Jalalvand, Ali R. [Faculty of Chemistry, Razi University, Kermanshah 671496734 (Iran, Islamic Republic of); Laboratorio de Desarrollo Analítico y Quimiometría (LADAQ), Cátedra de Química Analítica I, Universidad Nacional del Litoral, Ciudad Universitaria, CC 242 (S3000ZAA), Santa Fe (Argentina); Goicoechea, Hector C. [Laboratorio de Desarrollo Analítico y Quimiometría (LADAQ), Cátedra de Química Analítica I, Universidad Nacional del Litoral, Ciudad Universitaria, CC 242 (S3000ZAA), Santa Fe (Argentina)

    2014-07-01

    For the first time, a novel, robust and very attractive statistical experimental design (ED) using minimum-run equireplicated resolution IV factorial design (Min-Run Res IV FD) coupled with face centered central composite design (FCCCD) and Derringer's desirability function (DF) was developed to fabricate a highly selective and sensitive amperometric nitrite sensor based on electrodeposition of CoNi bimetallic alloy nanoparticles (NPs) on electrochemically reduced graphene oxide (ERGO) nanosheets. The modifications were characterized by cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), energy dispersive X-ray spectroscopic (EDS), scanning electron microscopy (SEM) techniques. The CoNi bimetallic alloy NPs were characterized using digital image processing (DIP) for particle counting (density estimation) and average diameter measurement. Under the identified optimal conditions, the novel sensor detects nitrite in concentration ranges of 0.1–30.0 μM and 30.0–330.0 μM with a limit of detection (LOD) of 0.05 μM. This sensor selectively detects nitrite even in the presence of high concentration of common ions and biological interferents therefore, we found that the sensor is highly selective. The sensor also demonstrated an excellent operational stability and good antifouling properties. The proposed sensor was used to the determination of nitrite in several foodstuff and water samples. - Highlights: • Eight variables were screened by Min Run Res IV FD to identify the key variables. • Mathematical models for the two studied responses were developed by FCCCD. • By using DF the responses were optimized simultaneously. • The SEM image of the modified electrode was processed by digital image processing. • The sensor was successfully applied to determination of nitrite in real samples.

  16. Microfluidic electrochemical reactors

    Science.gov (United States)

    Nuzzo, Ralph G [Champaign, IL; Mitrovski, Svetlana M [Urbana, IL

    2011-03-22

    A microfluidic electrochemical reactor includes an electrode and one or more microfluidic channels on the electrode, where the microfluidic channels are covered with a membrane containing a gas permeable polymer. The distance between the electrode and the membrane is less than 500 micrometers. The microfluidic electrochemical reactor can provide for increased reaction rates in electrochemical reactions using a gaseous reactant, as compared to conventional electrochemical cells. Microfluidic electrochemical reactors can be incorporated into devices for applications such as fuel cells, electrochemical analysis, microfluidic actuation, pH gradient formation.

  17. Synthesis of new chlorin e6 trimethyl and protoporphyrin IX dimethyl ester derivatives and their photophysical and electrochemical characterizations.

    Science.gov (United States)

    Menezes, José C J M D S; Faustino, M Amparo F; de Oliveira, Kleber T; Uliana, Marciana P; Ferreira, Vitor F; Hackbarth, Steffen; Röder, Beate; Teixeira Tasso, Thiago; Furuyama, Taniyuki; Kobayashi, Nagao; Silva, Artur M S; Neves, M Graça P M S; Cavaleiro, José A S

    2014-10-13

    In view of increasing demands for efficient photosensitizers for photodynamic therapy (PDT), we herein report the synthesis and photophysical characterizations of new chlorin e6 trimethyl ester and protoporphyrin IX dimethyl ester dyads as free bases and Zn(II) complexes. The synthesis of these molecules linked at the β-pyrrolic positions to pyrano[3,2-c]coumarin, pyrano[3,2-c]quinolinone, and pyrano[3,2-c]naphthoquinone moieties was performed by using the domino Knoevenagel hetero Diels-Alder reaction. The α-methylenechromanes, α-methylenequinoline, and ortho-quinone methides were generated in situ from a Knoevenagel reaction of 4-hydroxycoumarin, 4-hydroxy-6-methylcoumarin, 4-hydroxy-N-methylquinolinone, and 2-hydroxy-1,4-naphthoquinone, respectively, with paraformaldehyde in dioxane. All the dyads as free bases and as Zn(II) complexes were obtained in high yields. All new compounds were fully characterized by 1D and 2D NMR techniques, UV/Vis spectroscopy, and HRMS. Their photophysical properties were evaluated by measuring the fluorescence quantum yield, the singlet oxygen quantum yield by luminescence detection, and also the triplet lifetimes were correlated by flash photolysis and intersystem crossing (ISC) rates. The fluorescence lifetimes were measured by a time-correlated single photon count (TCSPC) method, fluorescence decay associated spectra (FDAS), and anisotropy measurements. Magnetic circular dichroism (MCD) and circular dichroism (CD) spectra were recorded for one Zn(II) complex in order to obtain information, respectively, on the electronic and conformational states, and interpretation of these spectra was enhanced by molecular orbital (MO) calculations. Electrochemical studies of the Zn(II) complexes were also carried out to gain insights into their behavior for such applications. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  18. Novel Co{sub 3}O{sub 4} porous polyhedrons derived from metal–organic framework toward high performance for electrochemical energy devices

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Youcun, E-mail: chenyc@aqtc.edu.cn [Anqing Normal College, School of Chemistry and Chemical Engineering, Anqing 246011 (China); Hu, Lin [High Magnetic Field Laboratory, Chinese Academy of Sciences, Hefei 230031 (China)

    2016-07-15

    Co{sub 3}O{sub 4} polyhedrons with porous structure have been synthesized simply by annealing Prussian blue analogue (PBA) Co{sub 3}[Co(CN){sub 6}]{sub 2} polyhedrons at 400 °C in air. The product was characterized by a series of techniques, such as X-ray Diffraction (XRD), Field Emission Scanning Electron Microscopy (FESEM), Transmission Electron Microscopy (TEM), High-resolution TEM (HRTEM), X-ray Photoelectron Spectroscopy (XPS), and Brunauer–Emmett–Teller (BET) gas adsorption. Interestingly, when evaluated as an anode material for lithium-ion batteries (LIBs), the Co{sub 3}O{sub 4} porous polyhedrons manifested high reversible capacity (about 1200 mAh g{sup −1} at 50 mA g{sup −1}) and excellent cycling performance. Moreover, they also exhibited a high specific capacitance of 110 Fg{sup −1} when used as an electrode in the supercapacitor. It is suggested that the special morphology and porous nanostructure lead to the promising electrochemical properties. - Graphical abstract: Novel and complicated mesoporous architectures of Co{sub 3}O{sub 4} have been fabricated by thermal decomposition of Prussian Blue Analog (PBA) Co{sub 3}[Co(CN){sub 6}]{sub 2} polyhedrons which obtained at the room temperature. When Co{sub 3}O{sub 4} product was evaluated for Li-ion batteries (LIBs), they exhibited high reversible capacity of 1000 mAh g{sup −1} with excellent cycle life because of the hollow/porous structure. Display Omitted.

  19. Spatial distribution, temporal variation and risks of parabens and their chlorinated derivatives in urban surface water in Beijing, China

    Energy Technology Data Exchange (ETDEWEB)

    Li, Wenhui; Gao, Lihong [School of Chemistry and Biological Engineering, University of Science and Technology Beijing, Beijing 100083 (China); Shi, Yali; Wang, Yuan [State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Science, Chinese Academy of Sciences, Beijing 100085 (China); Liu, Jiemin, E-mail: liujm@ustb.edu.cn [School of Chemistry and Biological Engineering, University of Science and Technology Beijing, Beijing 100083 (China); Cai, Yaqi, E-mail: caiyaqi@rcees.ac.cn [State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Science, Chinese Academy of Sciences, Beijing 100085 (China)

    2016-01-01

    The occurrence and distribution of 13 target compounds, including eight parabens, four chlorinated parabens and p-hydroxybenzoic acid (PHBA), were detected in surface water samples at 35 sampling sites in the Beijing River system, China. The surface water samples were collected from the main rivers and lakes in the urban area monthly from July 2013 to June 2014 (except the frozen period). Laboratory analyses revealed that parabens were ubiquitous in the surface water of Beijing. PHBA was the predominant compound in the surface water samples, with the average concentration of 239 ng L{sup −1}, followed by the total amount of chlorinated parabens (average 50.1 ng/L) and parabens (average 44.3 ng/L). It is noteworthy that octylparaben with longer chain was firstly detected in the surface water. Significant difference was observed for paraben concentrations from different sampling sites, and the highest level of parabens was found in the Xiaotaihou River, which was mainly due to the untreated sewage discharge. Seasonal variation of target compounds in the urban surface water was also studied, and parabens exhibited a different temporal variation from chlorinated derivatives. A combination of factors including high residual chlorine level and water temperature as well as intense ultraviolet radiation might enhance the persistence of chlorinated parabens in chlorinated water during the wet season. Risk assessment showed that parabens and their chlorinated derivatives are not likely to produce biological effects on aquatic ecosystems at current levels in the surface water of Beijing. - Highlights: • Parabens and chlorinated parabens are ubiquitous in surface water in Beijing. • Octylparaben with longer chain was firstly detected in surface water. • Untreated sewage discharge was the main source of parabens in river. • Parabens exhibited a different seasonal variation from chlorinated derivatives. • The risks of target compounds are negligible at

  20. Electrochemical promotion of catalytic reactions

    Science.gov (United States)

    Imbihl, R.

    2010-05-01

    The electrochemical promotion of heterogeneously catalyzed reactions (EPOC) became feasible through the use of porous metal electrodes interfaced to a solid electrolyte. With the O 2- conducting yttrium stabilized zirconia (YSZ), the Na + conducting β″-Al 2O 3 (β-alumina), and several other types of solid electrolytes the EPOC effect has been demonstrated for about 100 reaction systems in studies conducted mainly in the mbar range. Surface science investigations showed that the physical basis for the EPOC effect lies in the electrochemically induced spillover of oxygen and alkali metal, respectively, onto the surface of the metal electrodes. For the catalytic promotion effect general concepts and mechanistic schemes were proposed but these concepts and schemes are largely speculative. Applying surface analytical tools to EPOC systems the proposed mechanistic schemes can be verified or invalidated. This report summarizes the progress which has been achieved in the mechanistic understanding of the EPOC effect.

  1. Accuracy of linear measurements from cone-beam computed tomography-derived surface models of different voxel sizes

    NARCIS (Netherlands)

    Damstra, Janalt; Fourie, Zacharias; Huddleston Slater, James J R; Ren, Yijin

    INTRODUCTION: The aims of this study were to determine the linear accuracy of 3-dimensional surface models derived from a commercially available cone-beam computed tomography (CBCT) dental imaging system and volumetric rendering software and to investigate the influence of voxel resolution on the

  2. Segmentation process significantly influences the accuracy of 3D surface models derived from cone beam computed tomography

    NARCIS (Netherlands)

    Fourie, Zacharias; Damstra, Janalt; Schepers, Rutger H; Gerrits, Pieter; Ren, Yijin

    AIMS: To assess the accuracy of surface models derived from 3D cone beam computed tomography (CBCT) with two different segmentation protocols. MATERIALS AND METHODS: Seven fresh-frozen cadaver heads were used. There was no conflict of interests in this study. CBCT scans were made of the heads and 3D

  3. Organic-inorganic hybrid superhydrophobic surfaces using methyltriethoxysilane and tetraethoxysilane sol-gel derived materials in emulsion

    Science.gov (United States)

    Wen, Xiu-Fang; Wang, Kun; Pi, Pi-Hui; Yang, Jin-Xin; Cai, Zhi-Qi; Zhang, Li-juan; Qian, Yu; Yang, Zhuo-Ru; Zheng, Da-feng; Cheng, Jiang

    2011-11-01

    By applying alkaline-catalyzed co-hydrolysis and copolycondensation reactions of tetraethoxysilane (TEOS) and methyltriethoxysilane (MTES) in organic siloxane modified polyacrylate emulsion (OSPA emulsion), we are able to demonstrate the potential for developing a sol-gel derived organic-inorganic hybrid emulsion for a superhydrophobic surface research. TEOS and MTES derived sol-gel moieties can be designed for a physical roughness and hydrophobic characteristic (Si-CH3) of the hybrid superhydrophobic surface, while OSPA emulsion can be endowed for good film-forming property. The effect of formulation parameters on superhydrophobicity and film-forming property was analyzed. The water contact angle (WCA) on the sol-gel derived hybrid film is determined to be 156°, and the contact angle hysteresis is 5° by keeping the mole ratio of TEOS:MTES:C2H5OH:NH3·H2O:AMP-95 at 1:4:30:10:0.63 and the mass percentage of OSPA emulsion at 25%. The nanoparticle-based silica rough surface is observed as the mole ratio of MTES/TEOS at 4:1. The sol-gel derived organic-inorganic hybrid emulsion shows remarkable film-forming property when the mole ratio of MTES/TEOS reaches or exceeds 4:1. With the primer coating, the performance of superhydrophobic film achieve actual use standard. It reveals that this new procedure is an effective shortcut to obtain a superhydrophobic surface with potential applications.

  4. Using Electronic Energy Derivative Information in Automated Potential Energy Surface Construction for Vibrational Calculations.

    Science.gov (United States)

    Sparta, Manuel; Hansen, Mikkel B; Matito, Eduard; Toffoli, Daniele; Christiansen, Ove

    2010-10-12

    The availability of an accurate representation of the potential energy surface (PES) is an essential prerequisite in an anharmonic vibrational calculation. At the same time, the high dimensionality of the fully coupled PES and the adverse scaling properties with respect to the molecular size make the construction of an accurate PES a computationally demanding task. In the past few years, our group tested and developed a series of tools and techniques aimed at defining computationally efficient, black-box protocols for the construction of PESs for use in vibrational calculations. This includes the definition of an adaptive density-guided approach (ADGA) for the construction of PESs from an automatically generated set of evaluation points. Another separate aspect has been the exploration of the use of derivative information through modified Shepard (MS) interpolation/extrapolation procedures. With this article, we present an assembled machinery where these methods are embedded in an efficient way to provide both a general machinery as well as concrete computational protocols. In this framework we introduce and discuss the accuracy and computational efficiency of two methods, called ADGA[2gx3M] and ADGA[2hx3M], where the ADGA recipe is used (with MS interpolation) to automatically define modest sized grids for up to two-mode couplings, while MS extrapolation based on, respectively, gradients only and gradients and Hessians from the ADGA determined points provides access to sufficiently accurate three-mode couplings. The performance of the resulting potentials is investigated in vibrational coupled cluster (VCC) calculations. Three molecular systems serve as benchmarks: a trisubstituted methane (CHFClBr), methanimine (CH2NH), and oxazole (C3H3NO). Furthermore, methanimine and oxazole are addressed in accurate calculations aiming to reproduce experimental results.

  5. Solving atomic structures using statistical mechanical searches on x-ray scattering derived potential energy surfaces

    Science.gov (United States)

    Wright, Christopher James

    Engineering the next generation of materials, especially nanomaterials, requires a detailed understanding of the material's underlying atomic structure. These structures give us better insight into structure-property relationships, allowing for property driven material design on the atomic level. Even more importantly, understanding structures in-situ will translate stimuli and responses on the macroscopic scale to changes on the nanoscale. Despite the importance of precise atomic structures for materials design, solving atomic structures is difficult both experimentally and computationally. Atomic pair distribution functions (PDFs) provide information on atomic structure, but the difficulty of extracting the PDF from x-ray total scattering measurements limits their use. Translating the PDF into an atomic structure requires the search of a very high dimensional space, the set of all potential atomic configurations. The large computational cost of running these simulations also limits the use of PDF as an atomistic probe. This work aims to address these issues by developing 1) novel statistical mechanical approaches to solving material structures, 2) fast simulation of x-ray total scattering and atomic pair distribution functions (PDFs), and 3) data processing procedures for experimental x-ray total scattering measurements. First, experimentally derived potential energy surfaces (PES) and the statistical mechanical ensembles used to search them are developed. Then the mathematical and computational framework for the PDF and its gradients will be discussed. The combined PDF-PES-ensemble system will be benchmarked against a series of nanoparticle structures to ascertain the efficiency and effectiveness of the system. Experimental data processing procedures, which maximize the usable data, will be presented. Finally, preliminary results from experimental x-ray total scattering measurements will be discussed. This work presents one of the most complete end

  6. 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.

  7. Electrochemical kinetics theoretical aspects

    CERN Document Server

    Vetter, Klaus J

    1967-01-01

    Electrochemical Kinetics: Theoretical Aspects focuses on the processes, methodologies, reactions, and transformations in electrochemical kinetics. The book first offers information on electrochemical thermodynamics and the theory of overvoltage. Topics include equilibrium potentials, concepts and definitions, electrical double layer and electrocapillarity, and charge-transfer, diffusion, and reaction overvoltage. Crystallization overvoltage, total overvoltage, and resistance polarization are also discussed. The text then examines the methods of determining electrochemical reaction mechanisms

  8. Satellite-derived surface and sub-surface water storage in the Ganges–Brahmaputra River Basin

    Directory of Open Access Journals (Sweden)

    Fabrice Papa

    2015-09-01

    New hydrological insights: Basin-scale monthly SWS variations for the period 2003–2007 show a mean annual amplitude of ∼410 km3, contributing to about 45% of the Gravity Recovery And Climate Experiment (GRACE-derived total water storage variations (TWS. During the drought-like conditions in 2006, we estimate that the SWS deficit over the entire GB basin in July–August–September was about 30% as compared to other years. The SWS variations are then used to decompose the GB GRACE-derived TWS and isolate the variations of SSWS whose mean annual amplitude is estimated to be ∼550 km3. This new dataset of water storage variations represent an unprecedented source of information for hydrological and climate modeling studies of the ISC.

  9. Fabrication of a Microneedle/CNT Hierarchical Micro/Nano Surface Electrochemical Sensor and Its In-Vitro Glucose Sensing Characterization

    OpenAIRE

    Youngsam Yoon; Lee, Gil S.; Koangki Yoo; Jeong-Bong Lee

    2013-01-01

    We report fabrication of a microneedle-based three-electrode integrated electrochemical sensor and in-vitro characterization of this sensor for glucose sensing applications. A piece of silicon was sequentially dry and wet etched to form a 15 × 15 array of tall (approximately 380 µm) sharp silicon microneedles. Iron catalyst was deposited through a SU-8 shadow mask to form the working electrode and counter electrode. A multi-walled carbon nanotube forest was grown directly on the silicon micr...

  10. Electrochemical cell structure including an ionomeric barrier

    Science.gov (United States)

    Lambert, Timothy N.; Hibbs, Michael

    2017-06-20

    An apparatus includes an electrochemical half-cell comprising: an electrolyte, an anode; and an ionomeric barrier positioned between the electrolyte and the anode. The anode may comprise a multi-electron vanadium phosphorous alloy, such as VP.sub.x, wherein x is 1-5. The electrochemical half-cell is configured to oxidize the vanadium and phosphorous alloy to release electrons. A method of mitigating corrosion in an electrochemical cell includes disposing an ionomeric barrier in a path of electrolyte or ion flow to an anode and mitigating anion accumulation on the surface of the anode.

  11. Synthesis, antibacterial and surface activity of 1,2,4-triazole derivatives

    Directory of Open Access Journals (Sweden)

    El-Sayed, R.

    2006-06-01

    Full Text Available The use of sodium 1-(4-amino-5-mercapto-4H-[1,2,4] triazol-3-yl and heptadecane-1-sulfonate (2 as new precursors to synthesize some important biologically active heterocycles has been found to be effective. The reaction of 2 with carbon disulphide in pyridine and acid chlorides yielded the 1,2,4-triazole derivatives 3, 4a and 4b.The condensation of 2 with appropriate aldehydes gave 5a-c which were cyclized by treating with thioglycollic acid to yield 6a-c. The reactions of 2 with phthalic anhydride and 4-methylbenzene-sulfonylchloride gave 7 and 8. In addition, the reaction of 2 with chloroacetaldehyde, phenacyl bromide, urea and chloroacetyl chloride yielded 9, 10, 11 and 12. At the same time, refluxing 2 with phenyl isothiocyanate gave 13 and 14. All these products have antimicrobial activity and they can be used as surface active agents.Es interesante el uso del 1-(4-amino-5-mercapto-4H- [1,2,4]triazol-3-ilheptadecano-1-sulfonato sódico (2 como un nuevo precursor en la síntesis de compuestos heterocíclicos biológicamente importantes. La reacción de 2 con disulfuro de carbono en piridina y cloruros de acilo rindió derivados 1,2,4-triazólicos. Condensación de 2 con aldehídos apropiados produjo 5a-c que ciclaron por tratamiento con ácido tioglicólico para dar lugar a 6a-c. Reacciones de 2 con anhídrido ftálico y cloruro de 4-metilbenzenosulfonilo produjeron 7 y 8. Además, la reacción de 2 con cloroacetaldehído, bromuro de fenacilo, urea, cloruro de tiacetilo produjo 9, 10, 11, y 12. Por otra parte, el reflujo de 2 con isocianato de fenilo dio 13 y 14. Todos los productos tuvieron actividad antimicrobiana y propiedades tensoactivas.

  12. The annual cycle of satellite derived sea surface temperature on the western South Atlantic shelf

    Directory of Open Access Journals (Sweden)

    Carlos A. D. Lentini

    2000-01-01

    Full Text Available In this article, thirteen years of weekly sea surface temperature (SST fields derived from NOAA Advanced Very High Resolution Radiometer global area coverage infrared satellite data, from January 1982 to December 1994, are used to investigate spatial and temporal variabilities of SST seasonal cycle in the Southwest Atlantic Oceano This work addresses large scale variations over the eastem South American continental shelf and slope regions limited offshore by the 1000-m isobath, between 42° and 22°S. SST time series are fit with annual and semi-annual harmonics to describe the annual variation of sea surface temperatures. The annual harmonic explains a large proportion of the SST variability. The coefficient of determination is highest (> 90% on the continental shelf, decreasing offshore. The estimated amplitude of the seasonal cycle ranges between 4° and 13°e throughout the study area, with minima in August­September and maxima in February-March. After the identification and removal of the dominant annual components ofSST variability, models such as the one presented here are an attractive tool to study interannual SST variability.Neste artigo, treze anos de imagens semanais da temperatura da superfície do mar (TSM obtidas através do sensor infravermelho Advanced Very High Resolution Radiometer a bordo dos satélites NOAA, de janeiro de 1982 a dezembro de 1994, são utlilizadas para investigar as variabilidades espacial e temporal do cicIo sazonal de TSM no Oceano Atlântico Sudoeste. Este trabalho objetiva as variações de larga escala sobre a plataforma continental e o talude leste da América do Sul limitados ao largo pela isóbata de 1000 metros, entre 42°5 e 22°S. As séries temporais de TSM são ajustadas aos .harmônicos anual e sem i-anual para descrever a variação anual das temperaturas da superfície do mar. O harmônico anual explica a maior parte da variabilidade da TSM. O coeficiente de determinação é alto (> 90

  13. Heteroatom Polymer-Derived 3D High-Surface-Area and Mesoporous Graphene Sheet-Like Carbon for Supercapacitors.

    Science.gov (United States)

    Sheng, Haiyang; Wei, Min; D'Aloia, Alyssa; Wu, Gang

    2016-11-09

    Current supercapacitors suffer from low energy density mainly due to the high degree of microporosity and insufficient hydrophilicity of their carbon electrodes. Development of a supercapacitor capable of simultaneously storing as much energy as a battery, along with providing sufficient power and long cycle stability would be valued for energy storage applications and innovations. Differing from commonly studied reduced graphene oxides, in this work we identified an inexpensive heteroatom polymer (polyaniline-PANI) as a carbon/nitrogen precursor, and applied a controlled thermal treatment at elevated temperature to convert PANI into 3D high-surface-area graphene-sheet-like carbon materials. During the carbonization process, various transition metals including Fe, Co, and Ni were added, which play critical roles in both catalyzing the graphitization and serving as pore forming agents. Factors including post-treatments, heating temperatures, and types of metal were found crucial for achieving enhanced capacitance performance on resulting carbon materials. Using FeCl3 as precursor along with optimal heating temperature 1000 °C and mixed acid treatment (HCl+HNO3), the highest Brunauer-Emmett-Teller (BET) surface area of 1645 m(2)g(-1) was achieved on the mesopore dominant graphene-sheet-like carbon materials. The unique morphologies featured with high-surface areas, dominant mesopores, proper nitrogen doping, and 3D graphene-like structures correspond to remarkably enhanced electrochemical specific capacitance up to 478 Fg(-1) in 1.0 M KOH at a scan rate of 5 mV s(-1). Furthermore, in a real two-electrode system of a symmetric supercapacitor, a specific capacitance of 235 Fg(-1) using Nafion binder is obtained under a current density of 1 Ag(-1) by galvanostatic charge-discharge tests in 6.0 M KOH. Long-term cycle stability up to 5000 cycles by using PVDF binder in electrode was systematically evaluated as a function of types of metals and current densities.

  14. Electrochemical and thermal studies of lithium ion batteries

    Science.gov (United States)

    Lu, Wenquan

    The structural, electrochemical, and thermal characteristics of carbonaceous anodes and LiNi0.8Co0.2O2 cathode in Li-ion cells were investigated using various electrochemical and calorimetric techniques. The electrode-electrolyte interface was investigated for various carbonaceous materials such as graphite with different shapes, surface modified graphite with copper, and novel carbon material derived from sepiolite template. The structural and morphological properties were determined using XRD, TGA, SEM, BET techniques. The electrochemical characteristics were studied using conventional electrochemical techniques such as galvanostatic charge/discharge cycling, cyclic voltammetry, and impedance (AC and DC) methods. It was observed that the electrochemical active surface area instead of the BET area plays a critical role in the irreversible capacity loss associated with the carbonaceous anodes. It was also found that the exfoliation of carbon anodes especially in PC based electrolyte could be significantly reduced by protective copper coating of the natural graphite. LiNi0.8Co0.2O2 cathode material was found to possess high energy density and excellent cycling characteristics. The structural and electrochemical properties of LiNi0.8Co 0.2O2 synthesized by sol-gel and solid-state methods were studied. Results of the AC impedance spectroscopy carried out on LiNi 0.8Co0.2O2 cathodes revealed that the charge transfer resistance is a function of the state of charge. The solid state Li + diffusion was calculated to be around 10-13 cm2/s in the oxide particle by Warburg impedance method. In addition, the cell fabricated with LiNi0.8Co0.2O 2 cathode showed excellent energy and power performance under static and dynamic load conditions that prevail in Electric and Hybrid Vehicles. Thermal properties of the LiNi0.8Co0.2O2 cathode, carbonaceous anodes, and Li-ion cells fabricated with these electrodes were also investigated using isothermal microcalorimetry (IMC), differential

  15. Ice particle habit and surface roughness derived from PARASOL polarization measurements

    OpenAIRE

    B. H. Cole; P. Yang; B. A. Baum; J. Riedi; L. C.-Labonnote

    2014-01-01

    Ice clouds are an important element in the radiative balance of the earth's climate system, but their microphysical and optical properties still are not well constrained, especially ice particle habit and the degree of particle surface roughness. In situ observations have revealed common ice particle habits and evidence for surface roughness, but these observations are limited. An alternative is to infer the ice particle shape and surface roughness from satellite observat...

  16. Application of Satellite-Derived Ocean Surface Winds to the Detection of Weather Systems and the Prediction of Near-Ocean Surface Winds around Hawaii

    Directory of Open Access Journals (Sweden)

    Hsi-Chyi Yeh

    2010-01-01

    Full Text Available The Hawaiian Island chain is surrounded by the open ocean and is an ideal place to conduct the application of QuikSCAT satellite-derived ocean surface winds to the detection of weather systems. With the help of QuikSCAT winds, the associated circulation of the weather systems over the open ocean around Hawaii can be identified. In this study, the obvious cyclonic circulation associated with a Kona storm, the significant wind shift and wind confluence related to the surface cold front, and the anticyclonic circulation related to high-pressure systems for both a strong-wind event and a trade-wind condition are revealed over the open ocean through QuikSCAT winds. The propagation of a cold frontal boundary, defined by the wind shift and wind confluence, also can be clearly detected using the reanalyzed ocean-surface winds.

  17. Improving Mean Minimum and Maximum Month-to-Month Air Temperature Surfaces Using Satellite-Derived Land Surface Temperature

    Directory of Open Access Journals (Sweden)

    Maria Mira

    2017-12-01

    Full Text Available Month-to-month air temperature (Tair surfaces are increasingly demanded to feed quantitative models related to a wide range of fields, such as hydrology, ecology or climate change studies. Geostatistical interpolation techniques provide such continuous and objective surfaces of climate variables, while the use of remote sensing data may improve the estimates, especially when temporal resolution is detailed enough. The main goal of this study is to propose an empirical methodology for improving the month-to-month Tair mapping (minimum and maximum using satellite land surface temperatures (LST besides of meteorological data and geographic information. The methodology consists on multiple regression analysis combined with the spatial interpolation of residual errors using the inverse distance weighting. A leave-one-out cross-validation procedure has been included in order to compare predicted with observed values. Different operational daytime and nighttime LST products corresponding to the four months more characteristic of the seasonal dynamics of a Mediterranean climate have been considered for a thirteen-year period. The results can be considered operational given the feasibility of the models employed (linear dependence on predictors that are nowadays easily available, the robustness of the leave-one-out cross-validation procedure and the improvement in accuracy achieved when compared to classical Tair modeling results. Unlike what is considered by most studies, it is shown that nighttime LST provides a good proxy not only for minimum Tair, but also for maximum Tair. The improvement achieved by the inclusion of remote sensing LST products was higher for minimum Tair (up to 0.35 K on December, especially over forests and rugged lands. Results are really encouraging, as there are generally few meteorological stations in zones with these characteristics, clearly showing the usefulness of remote sensing to improve information about areas that are

  18. Plasmonic Imaging of Electrochemical Reactions of Single Nanoparticles.

    Science.gov (United States)

    Fang, Yimin; Wang, Hui; Yu, Hui; Liu, Xianwei; Wang, Wei; Chen, Hong-Yuan; Tao, N J

    2016-11-15

    Electrochemical reactions are involved in many natural phenomena, and are responsible for various applications, including energy conversion and storage, material processing and protection, and chemical detection and analysis. An electrochemical reaction is accompanied by electron transfer between a chemical species and an electrode. For this reason, it has been studied by measuring current, charge, or related electrical quantities. This approach has led to the development of various electrochemical methods, which have played an essential role in the understanding and applications of electrochemistry. While powerful, most of the traditional methods lack spatial and temporal resolutions desired for studying heterogeneous electrochemical reactions on electrode surfaces and in nanoscale materials. To overcome the limitations, scanning probe microscopes have been invented to map local electrochemical reactions with nanometer resolution. Examples include the scanning electrochemical microscope and scanning electrochemical cell microscope, which directly image local electrochemical reaction current using a scanning electrode or pipet. The use of a scanning probe in these microscopes provides high spatial resolution, but at the expense of temporal resolution and throughput. This Account discusses an alternative approach to study electrochemical reactions. Instead of measuring electron transfer electrically, it detects the accompanying changes in the reactant and product concentrations on the electrode surface optically via surface plasmon resonance (SPR). SPR is highly surface sensitive, and it provides quantitative information on the surface concentrations of reactants and products vs time and electrode potential, from which local reaction kinetics can be analyzed and quantified. The plasmonic approach allows imaging of local electrochemical reactions with high temporal resolution and sensitivity, making it attractive for studying electrochemical reactions in biological

  19. Effect of surface treatment on electrochemical properties of TiMn 1.6Ni 0.4 alloy in alkaline electrolyte

    Science.gov (United States)

    Ramya, K.; Rajalakshmi, N.; Sridhar, P.; Sivasankar, B.

    The characteristic features of the electrochemical behaviour of the treated hydrogen-storage alloy TiMn 1.6Ni 0.4 in an etching solution containing hydrogen fluoride and untreated alloy in alkaline media are investigated. Alloy characteristics such as discharge capacity, high-rate dischargebility and cycle-life are examined. The exchange current density, polarisation resistance and diffusion coefficients are also determined as functions of state-of-charge of the electrodes. The diffusion coefficient is found to be of the same order for the treated and the untreated alloy.

  20. Investigation of the corrosion resistance of Ti-13Nb-13Zr alloy by electrochemical techniques and surface analysis; Investigacao da resistencia a corrosao da liga Ti-13Nb-13Zr por meio de tecnicas eletroquimicas e de analise de superficie

    Energy Technology Data Exchange (ETDEWEB)

    Assis, Sergio Luiz de

    2006-07-01

    In this work, the in vitro corrosion resistance of the Ti-13Nb-13Zr alloy, manufactured at a national laboratory, and used for orthopedic applications, has been investigated in solutions that simulate the body fluids. The electrolytes used were 0.9 % (mass) NaCl, Hanks' solution, a culture medium (MEM), and the two last electrolytes, without and with addition of hydrogen peroxide. The aim of peroxide addition was to simulate the conditions found when inflammatory reactions occur due to surgical procedures. The corrosion resistance of alloys commercially in use as biomaterials, Ti-6Al-7Nb and Ti-6Al-4V, as well as of the pure titanium (Ti-cp), was also studied for comparison with the Ti-13Nb-13Zr alloy. The corrosion resistance characterization was carried out by electrochemical and surface analysis techniques. The electrochemical tests used were: open circuit potential measurements as a function of tim; potentiodynamic polarization; and electrochemical impedance spectroscopy (EIE). The impedance experimental diagrams were interpreted using equivalent electric circuits that simulate an oxide film with a duplex structure composed of an internal and compact, barrier type layer, and an external porous layer. The results showed that the corrosion resistance is due mainly to the barrier type layer. The titanium alloys and the Ti-cp showed high corrosion resistance in all electrolytes used. The oxides formed on the Ti-13Nb-13Zr, either naturally or during immersion in MEM ar Hank's solution was characterized by X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (MEV). The results showed that the presence of hydrogen peroxide in MEM promotes the growth of the porous layer and incorporation of mineral ions, besides favouring hydroxyapatite formation. The cytotoxicity of the Ti-13Nb-13Zr alloy was also evaluated and it was shown to be non-toxic. (author)

  1. Multifractal and Singularity Maps of soil surface moisture distribution derived from 2D image analysis.

    Science.gov (United States)

    Cumbrera, Ramiro; Millán, Humberto; Martín-Sotoca, Juan Jose; Pérez Soto, Luis; Sanchez, Maria Elena; Tarquis, Ana Maria

    2016-04-01

    methods for mapping geochemical anomalies caused by buried sources and for predicting undiscovered mineral deposits in covered areas. Journal of Geochemical Exploration, 122, 55-70. Cumbrera, R., Ana M. Tarquis, Gabriel Gascó, Humberto Millán (2012) Fractal scaling of apparent soil moisture estimated from vertical planes of Vertisol pit images. Journal of Hydrology (452-453), 205-212. Martin Sotoca; J.J. Antonio Saa-Requejo, Juan Grau and Ana M. Tarquis (2016). Segmentation of singularity maps in the context of soil porosity. Geophysical Research Abstracts, 18, EGU2016-11402. Millán, H., Cumbrera, R. and Ana M. Tarquis (2016) Multifractal and Levy-stable statistics of soil surface moisture distribution derived from 2D image analysis. Applied Mathematical Modelling, 40(3), 2384-2395.

  2. 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.

  3. High performance electrochemical pseudocapacitors from ionic liquid assisted electrochemically synthesized p-type conductive polymer.

    Science.gov (United States)

    Ehsani, A; Mohammad Shiri, H; Kowsari, E; Safari, R; Torabian, J; Hajghani, S

    2017-03-15

    In this paper firstly, 1-methyl-3-methylimidazolium bromide (MB) as a new high efficient ionic liquid was synthesized using chemical approach and then fabricated POAP/MB films by electro-polymerization of POAP in the presence of MB to serve as the active electrode for electrochemical supercapacitor. Theoretical study (AIM) and electrochemical analysis have been used for characterization of ionic liquid and POAP/MB composite film. Different electrochemical methods including galvanostatic charge-discharge experiments, cyclic voltammetry and electrochemical impedance spectroscopy are carried out in order to investigate the performance of the system. This work introduces new most efficient materials for electrochemical redox capacitors with advantages including ease synthesis, high active surface area and stability in an aqueous electrolyte. Copyright © 2016 Elsevier Inc. All rights reserved.

  4. Effectiveness of a coral-derived surfacing material for reducing sediment production on unpaved roads, Schoffield barracks, Oahu, Hawaii.

    Science.gov (United States)

    Ziegler, Alan D; Sutherland, Ross A

    2006-01-01

    This study evaluated the effectiveness of two application rates of a coral-derived surfacing material for both traffic and nontraffic road conditions using simulated rainfall (110-120 mm h(-1) for 30-90 min) on 0.75-m (wide) x 5.0-m (long) plots of similar slope (roughly 0.1 m m(-1)). The coral is a locally available material that has been applied to unpaved roads surfaces on Schoffield Barracks, Oahu, Hawaii (USA), where this experiment was conducted. The simulations show that compared with a bare control plot, the coral-based surface application rates of 80 and 160 kg m(-2) (equivalent to only 10- and 20-mm thicknesses) reduced road sediment production by 75% and 95%, respectively, for nontraffic conditions. However, after two passes of the research vehicle during wet conditions, sediment production rates for the two coral treatments were not significantly different from those on the bare road plots. The overall effectiveness of the coral-derived surfacing material is unsatisfactory, primarily because the on-road surface thickness associated with the application rates tested was too small. These rates were selected to bracket those applied to training roads in the study area. Furthermore, the composition of the coral-based material does not facilitate the development of a sealed, erosion-resistant surface. When applied at the low rates tested, the coral material breaks down under normal traffic conditions, thereby losing its ability to counter shearing forces exerted by overland flow on long hillslopes where erosion measures are most needed. These simulations, combined with observations on roads in the study area, indicate that this material is not an appropriate road surfacing material for the site-at least for the low application rates examined. These results are preliminary; extended testing of higher applications rates at the hillslope scale under natural climate and traffic conditions is needed to better judge the effectiveness of this material over time.

  5. Synthesis, characterization and electrochemical behaviour of cobalt(II) and cobalt(III):O 2- complexes, respectively, with linear and tripodal tetradentate ligands derived from Schiff bases

    Science.gov (United States)

    Djebbar-Sid, S.; Benali-Baitich, O.; Deloume, J. P.

    2001-07-01

    New octahedral cobalt complexes with linear and tripodal tetradentate ligands derived from Schiff bases have been synthesized and characterized using elemental analysis, molar conductance, IR spectra, magnetic measurements, electronic and ESR spectra. The experimental results support the binding of linear ligands with two N and two O donor sites to cobalt ion. They show a square planar geometry and tripodal ligands coordinated to the metal ion by only one nitrogen atom, giving an arrangement of NO 3 donor groups, the other axial sites being occupied by the molecular oxygen and/or the aquo molecules. From the results of cyclic voltammetry it is shown that chelate structure and ligand geometry and electron donating effect of the ligand substituents are among the factors influencing the redox potentials of the complexes. Linear ligands lead to high-spin cobalt(II) complexes. They do not interact with dioxygen and stabilize the Co(II) state counter to their related Schiff-base complexes. The low-spin complexes with tripodal ligands are O 2 adducts and the configuration in these complexes is best formulated as [Co IIIO 2-].

  6. A Novel CuxO Nanoparticles@ZIF-8 Composite Derived from Core-Shell Metal-Organic Frameworks for Highly Selective Electrochemical Sensing of Hydrogen Peroxide.

    Science.gov (United States)

    Yang, Juan; Ye, Huili; Zhao, Faqiong; Zeng, Baizhao

    2016-08-10

    A novel core-shell heterostructure of CuxO nanoparticles@zeolitic imidazolate framework (CuxO NPs@ZIF-8) was successfully prepared through facile pyrolysis of a nanocrystalline copper-based metal-organic framework [nHKUST-1, i.e., Cu3(BTC)2 (BTC = 1,3,5-benzene-tricarboxylate)]@ZIF-8, based on the different thermal stability of the two metal-organic frameworks (MOFs). The small CuxO NPs derived from nHKUST-1 were uniformly dispersed inside the host material and provided active sites, while ZIF-8 kept the original structure as the molecular sieving shell. Owing to the proper pore shape and pore size of ZIF-8, H2O2 could diffuse through the shell, but bigger molecules could not pass. Thus, the composite material exhibited high selectivity when it was used to construct a H2O2 sensor. In addition, the sensor showed an extended linear detection range (from 1.5 to 21442 μM), low detection limit (0.15 μM), and high sensitivity, due to the good electrocatalysis of CuxO NPs and the synergistic effect of the core-shell structure.

  7. Surface circulation in the Iroise Sea (western Brittany) derived from high resolution current mapping by HF radars

    Science.gov (United States)

    Sentchev, Alexei; Forget, Philippe; Barbin, Yves; Marié, Louis; Ardhuin, Fabrice

    2010-05-01

    The use of high frequency radar (HFR) systems for near-real-time coastal ocean monitoring necessities that short time scale motions of the radar-derived velocities are better understood. While the ocean radar systems are able to describe coastal flow patterns with unprecedented details, the data they produce are often too sparse or gappy for applications such as the identification of coherent structures and fronts or understanding transport and mixing processes. In this study, we address two challenges. First, we report results from the HF radar system (WERA) which is routinely operating since 2006 on the western Brittany coast to monitor surface circulation in the Iroise Sea, over an area extending up to 100 km offshore. To obtain more reliable records of vector current fields at high space and time resolution, the Multiple Signal Classification (MUSIC) direction finding algorithm is employed in conjunction with the variational interpolation (2dVar) of radar-derived velocities. This provides surface current maps at 1 km spacing and time resolution of 20 min. Removing the influence of the sea state on radar-derived current measurements is discussed and performed on some data sequences. Second, we examine in deep continuous 2d velocity records for a number of periods, exploring the different modes of variability of surface currents in the region. Given the extent, duration, and resolution of surface current velocity measurements, new quantitative insights from various time series and spatial analysis on higher frequency kinematics will be discussed. By better characterizing the full spectrum of flow regimes that contribute to the surface currents and their shears, a more complete picture of the circulation in the Iroise Sea can be obtained.

  8. Distribution of icy particles across Enceladus' surface as derived from Cassini-VIMS measurements

    Science.gov (United States)

    Jaumann, R.; Stephan, K.; Hansen, G.B.; Clark, R.N.; Buratti, B.J.; Brown, R.H.; Baines, K.H.; Newman, S.F.; Bellucci, G.; Filacchione, G.; Coradini, A.; Cruikshank, D.P.; Griffith, C.A.; Hibbitts, C.A.; McCord, T.B.; Nelson, R.M.; Nicholson, P.D.; Sotin, Christophe; Wagner, R.

    2008-01-01

    The surface of Enceladus consists almost completely of water ice. As the band depths of water ice absorptions are sensitive to the size of particles, absorptions can be used to map variations of icy particles across the surface. The Visual and Infrared Mapping Spectrometer (VIMS) observed Enceladus with a high spatial resolution during three Cassini flybys in 2005 (orbits EN 003, EN 004 and EN 011). Based on these data we measured the band depths of water ice absorptions at 1.04, 1.25, 1.5, and 2 ??m. These band depths were compared to water ice models that represent theoretically calculated reflectance spectra for a range of particle diameters between 2 ??m and 1 mm. The agreement between the experimental (VIMS) and model values supports the assumption that pure water ice characterizes the surface of Enceladus and therefore that variations in band depth correspond to variations in water ice particle diameters. Our measurements show that the particle diameter of water ice increases toward younger tectonically altered surface units with the largest particles exposed in relatively "fresh" surface material. The smallest particles were generally found in old densely cratered terrains. The largest particles (???0.2 mm) are concentrated in the so called "tiger stripes" at the south pole. In general, the particle diameters are strongly correlated with geologic features and surface ages, indicating a stratigraphic evolution of the surface that is caused by cryovolcanic resurfacing and impact gardening. ?? 2007 Elsevier Inc. All rights reserved.

  9. A superhydrophobic surface with high performance derived from STA-APTES organic-inorganic molecular hybrid.

    Science.gov (United States)

    Si, Fangfang; Zhao, Ning; Chen, Li; Xu, Jian; Tao, Qingsheng; Li, Jinyong; Ran, Chunbo

    2013-10-01

    The chemical originals of natural superhydrophobic surfaces are based on botanic or animal wax or fat, which have poor chemical and thermal resistance. Herein, we report a simple chemical modification of stearic acid (STA) with γ-aminopropyl triethoxysilane (APTES), to obtain an organic-inorganic molecular hybrid STA-APTES compound. A flower-like hierarchically structured surface with superhydrophobicity can be obtained simply by casting the STA-APTES solution under ambient circumstance. The crystallization of the hydrocarbon chain from STA leads to the formation of the binary microstructure and reduces the surface tension, contributing to the superhydrophobicity of the as-formed surface. In addition, the condensation of Si(OCH2CH3)3 from APTES can lead to the cross-linking of the resultant surface, which endows the as-formed superhydrophobic surface with high performances, such as excellent thermal and solvent resistance, etc. This superhydrophobic surface prepared is superior to its many analogs in nature, promising a wide application especially in harsh circumstance. Copyright © 2013 Elsevier Inc. All rights reserved.

  10. Electrochemical study of aluminum corrosion in boiling high purity water

    Science.gov (United States)

    Draley, J. E.; Legault, R. A.

    1969-01-01

    Electrochemical study of aluminum corrosion in boiling high-purity water includes an equation relating current and electrochemical potential derived on the basis of a physical model of the corrosion process. The work involved an examination of the cathodic polarization behavior of 1100 aluminum during aqueous oxidation.

  11. Fabrication of a microneedle/CNT hierarchical micro/nano surface electrochemical sensor and its in-vitro glucose sensing characterization.

    Science.gov (United States)

    Yoon, Youngsam; Lee, Gil S; Yoo, Koangki; Lee, Jeong-Bong

    2013-12-04

    We