247 research outputs found

    Passive Behavior and Passivity Breakdown of AISI 304 in LiBr Solutions through Scanning Electrochemical Microscopy

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    The passive behavior and passivity breakdown of AISI 304 stainless steel in LiBr solutions has been investigated by means of scanning electrochemical microscopy (SECM). The sample generation - tip collection (SG-TC) mode was used to operate the SECM and the tip potential was biased to detect the electroactive species. The evolution of the current at the ultramicroelectrode tip with the applied potential within the passive range was followed at different LiBr concentrations. Results show that the absolute value of the current at the tip increases with the applied potential. Additionally, SECM was also used to detect stable pits formed on the stainless steel surface in a 0.2 M LiBr solution. The results show clear evidence of the presence of high amounts of other reducible species (metal cations) apart from oxygen. Also, the dish-shape morphology of the pits observed using Confocal Laser Scanning Microscopy will be discussed in relation to the kinetics of the reactions observed using SECM. (c) 2014 The Electrochemical Society. All rights reserved.The authors would like to express their gratitude to the Generalitat Valenciana for its help in the SECM acquisition (PPC/2011/013) and in the CLSM acquisition (MY08/ISIRM/S/100) and to Dr. Asuncion Jaime for her translation assistance.Fernández Domene, RM.; Sánchez Tovar, R.; García Antón, J. (2014). Passive Behavior and Passivity Breakdown of AISI 304 in LiBr Solutions through Scanning Electrochemical Microscopy. Journal of The Electrochemical Society. 161(12):565-572. https://doi.org/10.1149/2.1051412jesS56557216112Cobb Harold M. (Ed.), Steel Products Manual: Stainless Steels, Iron & Steel Society, 1999.Schweitzer P. A. , Corrosion Engineering Handbook: Fundamentals of Metallic Corrosion, CRC Press, Boca Ratón, FL., 2007.Hakiki, N. 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    Enzymatic hydrolysis of esters from 2-carboxy-6- methoxy-2,3-dihydrobenzofuran acid

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    In this work we describe the results of the enzymatic hydrolysis of esters from 2-carboxy-6-methoxy-2,3-dihydrobenzofuran acid using Candida antarctica lipase supported on acrylic resin, with enantiomeric excesses ranging between 80 to 99%

    Effect of Reynolds number and lithium cation insertion on titanium anodization

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    This work studies the influence of using hydrodynamic conditions (Reynolds number, Re = 0 to Re = 600) during Ti anodization and Li+ intercalation on anatase TiO2 nanotubes. The synthesized photocatalysts were characterized by using Field Emission Scanning Electron Microscope (FE-SEM), Raman Confocal Laser Microscopy, Electrochemical Impedance Spectroscopy (EIS), Mott-Schottky analysis (M-S), photoelectrochemical hydrogen production and resistance to photocorrosion tests. The obtained results showed that the conductivity of the NTs increases with Li+ intercalation and Re. The latter is due to the fact that the hydrodynamic conditions eliminate part of the initiation layer formed over the tube-tops, which is related to an increase of the photocurrent in the photoelectrochemical water splitting. Besides, the photogenerated electron-hole pairs are facilitated by Li+ intercalation. Finally, this work confirms that there is a synergistic effect between Re and Li+ intercalation

    Directrices para zonificación, uso y manejo del desierto La Tatacoa

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    El Desierto de la Tatacoa se caracteriza por sus condiciones climáticas y botánicas de zonas tropicales áridas y semiáridas, cuyas tierras están dedicadas principalmente a la ganadería extensiva y en menor proporción a la agricultura. Sin embargo, sobresale por su riqueza paleontológica y sus áreas de refugio para la diversidad de aves en el alto Magdalena,  los atractivos naturales y aspectos sugerentes para el ecoturismo; éstos no son protegidos adecuadamente y en consecuencia, se ha considerado necesario proponer algunas directrices para su zonificación con fines de uso y manejo

    Synergistic effect between hydrodynamic conditions during Ti anodization and acidic treatment on the photoelectric properties of TiO2 nanotubes

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    In the present work, the combined influence of controlled hydrodynamic conditions during Ti anodization and the acidic treatment with HClO4 on the photoelectric properties of mixed anatase/rutile TiO2 nanotubes has been studied. Anodized samples were analyzed by means of Field Emission Scanning Electronic Microscopy (FE-SEM), Confocal Raman Microscopy, electrochemical measurements (electrochemical impedance spectroscopy and Mott-Schottky analysis) and photoelectrochemical measurements. It has been observed that the use of hydrodynamic conditions increases the surface area of nanotubes, while acidic treatment enhances their conductivity. Besides, there is a clear synergistic effect between the hydrodynamic conditions and the acidic treatment, which results in higher photocurrent densities for the treated nanotubes formed under hydrodynamic conditions.Authors would like to express their gratitude for the financial support to the Ministerio of Economia y Competitividad (Project CTQ2013-42494-R).Sánchez Tovar, R.; Fernández Domene, RM.; Martinez Sanchez, A.; Blasco Tamarit, ME.; García-Antón, J. (2015). Synergistic effect between hydrodynamic conditions during Ti anodization and acidic treatment on the photoelectric properties of TiO2 nanotubes. Journal of Catalysis. 330:434-441. https://doi.org/10.1016/j.jcat.2015.08.002S43444133

    Visible-light photoelectrodegradation of diuron on WO3 nanostructures

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    The degradation of pesticide diuron has been explored by photoelectrocatalysis (PEC) under visible light illumination using two different WO3 nanostructures, obtained by anodization of tungsten. The highest degradation efficiency (73%) was obtained for WO3 nanosheets synthesized in the presence of small amounts of hydrogen peroxide (0.05 M). For that nanostructure, the kinetic coefficient for diuron degradation was 133% higher than that for the other nanostructure (anodized in the presence of fluoride anions). These results have been explained by taking into account the different architecture and dimensions of the two WO3 nanostructures under study

    Charge disproportionation in YNiO3_{3} : ESR and susceptibility study

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    We present a study of the magnetic properties of YNiO3_{3} in the paramagnetic range, above and below the metal-insulator (MI) transition. The dc susceptibility, χdc\chi_{dc} (measured up to 1000 K) is a decreasing function of T for T>T >150 K (the N\'{e}el temperature) and we observe two different Curie-Weiss regimes corresponding to the metallic and insulator phases. In the metallic phase, this behaviour seems to be associated with the small ionic radius of Y% 3+^{3+}. The value of the Curie constant for T<< TMI_{MI} allows us to discard the possibility of Ni3+^{3+} localization. An electron spin resonance (ESR) spectrum is visible in the insulator phase and only a fraction of the Ni ions contributes to this resonance. We explain the ESR and χdc\chi _{dc} behaviour for T << TMI_{MI} in terms of charge disproportionation of the type 2Ni% ^{3+}\to Ni2+^{2+}+Ni4+,^{4+}, that is compatible with the previously observed structural transition across TMI_{MI}.Comment: 10 pages, 4 figures, submitted to Phys. Rev.

    Evidence of strong antiferromagnetic coupling between localized and itinerant electrons in ferromagnetic Sr2FeMoO6

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    Magnetic dc susceptibility (χ\chi) and electron spin resonance (ESR) measurements in the paramagnetic regime, are presented. We found a Curie-Weiss (CW) behavior for χ\chi(T) with a ferromagnetic Θ=446(5)\Theta = 446(5) K and μeff=4.72(9)μB/f.u.\mu_{eff} = 4.72(9) \mu_{B}/f.u., this being lower than that expected for either Fe3+(5.9μB)Fe^{3+}(5.9\mu_{B}) or Fe2+(4.9μB)Fe^{2+}(4.9\mu_{B}) ions. The ESR g-factor g=2.01(2)g = 2.01(2), is associated with Fe3+Fe^{3+}. We obtained an excellent description of the experiments in terms of two interacting sublattices: the localized Fe3+Fe^{3+} (3d53d^{5}) cores and the delocalized electrons. The coupled equations were solved in a mean-field approximation, assuming for the itinerant electrons a bare susceptibility independent on TT. We obtained χe0=3.7\chi_{e}^{0} = 3.7 10410^{-4} emu/mol. We show that the reduction of μeff\mu_{eff} for Fe3+Fe^{3+} arises from the strong antiferromagnetic (AFM) interaction between the two sublattices. At variance with classical ferrimagnets, we found that Θ\Theta is ferromagnetic. Within the same model, we show that the ESR spectrum can be described by Bloch-Hasegawa type equations. Bottleneck is evidenced by the absence of a gg-shift. Surprisingly, as observed in CMR manganites, no narrowing effects of the ESR linewidth is detected in spite of the presence of the strong magnetic coupling. These results provide evidence that the magnetic order in Sr2FeMoO6Sr_{2}FeMoO_{6} does not originates in superexchange interactions, but from a novel mechanism recently proposed for double perovskites
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