47 research outputs found

    Erratum to: 36th International Symposium on Intensive Care and Emergency Medicine

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    [This corrects the article DOI: 10.1186/s13054-016-1208-6.]

    Mechanism of passive layer formation on AA2024-T3 from alkaline lithium carbonate solutions in the presence of sodium chloride

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    This study focuses on the elucidation of the formation mechanism of passive layers on AA2024-T3 during the exposure to alkaline lithium carbonate solutions in the presence of sodium chloride. Under controlled conditions, in an electrochemical cell, a protective layer was generated comprising an amorphous inner layer and a crystalline outer-layer. In order to resolve the formation mechanism, the layers were characterized using surface analytical techniques to characterize the surface morphology, thickness and elemental composition of the layers at different stages of the formation process. In addition, electrochemical techniques were applied to link the electrochemical properties of the layers with the different stages of formation. The results demonstrate that the formation mechanism of these layers comprises three different stages: (I) oxide thinning, (II) anodic dissolution and film formation, followed by (III) film growth through a competitive growth-dissolution process. The passive properties of the layers are generated in the third stage through the densification of the amorphous layer. The combined results provide an enhanced insight in the formation mechanism and the development of the passive properties of these layers when lithium salts are used as leaching corrosion inhibitor for coated AA2024-T3.(OLD) MSE-6(OLD) MSE-

    Localised aqueous corrosion of electroless nickel immersion gold-coated copper

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    Electroless nickel (Ni) immersion gold (Au), commonly referred to by the acronym ENIG, is the most common protective coating applied on the exposed copper (Cu) traces of printed circuit boards (PCBs). In this work, we elucidate the local corrosion mechanism of the ENIG-Cu system by applying microscopic, surface analysis and electrochemical techniques with high spatial resolution to provide a comprehensive understanding of the complex local corrosion mechanism of the ENIG-Cu system. The corrosion initiation is highly localised and associated with pores or micro-defects in the Au layer. The corrosion initiates by the dissolution of the underlying Ni layer, being less noble than Au. The dissolution propagates in lateral and perpendicular directions relative to the surface in an elliptical fashion. With time, the direction of corrosion propagation changes to a predominantly lateral attack of the Ni layer. The corrosion process is governed by the cathode/anode ratio of the Au/Ni galvanic couple.Team Yaiza Gonzalez GarciaTeam Arjan Mo

    Benchmarking the Electrochemical CO<sub>2</sub> Reduction on Polycrystalline Copper Foils: The Importance of Microstructure Versus Applied Potential

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    Copper is one of the most promising catalysts for the CO2 reduction reaction (CO2RR) due to its unique capability of producing multicarbon products in appreciable quantities. Most of the CO2RR research efforts have been directed towards the development of new electrocatalysts to either increase product selectivities or decrease overpotentials. In contrast, only a few studies have systematically tested or benchmarked CO2RR performances of electrocatalysts. In this paper, for the first time, the performances of five different polycrystalline copper foils purchased from different suppliers are benchmarked for their CO2RR performance. Their differences are characterized in terms of microstructural features and the effect that these microstructural properties have on the electrocatalytic behavior during potentiostatic CO2RR experiments are evaluated. It is shown that the potential applied is the dominant factor controlling CO2RR selectivities, leading to the conclusion that microstructural properties of polycrystalline copper electrodes have a negligible effect on the outcome of CO2RR experiments.Large Scale Energy StorageTeam Amarante BottgerTeam Yaiza Gonzalez Garci

    Properties of Passive Films Formed on Ferrite-Martensite and Ferrite-Pearlite Steel Microstructures

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    The effect of ferrite-pearlite and ferrite-martensite phase combinations on the passive layer properties of low carbon steel is investigated in a 0.1 M NaOH solution. Heat treatments were designed to obtain ferrite-pearlite and ferrite-martensite microstructures with similar ferrite volume fractions. Potentiostatic polarisation and electrochemical impedance spectroscopy (EIS) results demonstrated the lower barrier properties of passive films on ferrite-martensite microstructure compared to the ones formed on ferrite-pearlite microstructure. This was attributed to the higher donor density of the passive layer on ferrite-martensite samples, measured with Mott–Schottky analysis. This behaviour was explained by the complex microstructure morphology of the martensite phase that led to the formation of a more defective passive filmTeam Yaiza Gonzalez GarciaTeam Jilt Sietsm

    Role of Grain Size and Recrystallization Texture in the Corrosion Behavior of Pure Iron in Acidic Medium

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    This work investigates the role of grain size and recrystallization texture in the corrosion behavior of pure iron in 0.1 M sulfuric acid solution. Annealing heat treatment was applied to obtain samples with different average grain sizes (26, 53 and 87 µm). Optical microscopy, X-ray diffraction and electron backscatter diffraction techniques were used to characterize the microstructure. The EBSD data analysis showed ferrite phase with no inclusions and very low geometrically necessary dislocation density, indicating strain-free grains constituting all samples. The crystallographic texture analysis of the samples revealed that the 26 µm grain size sample had a high volume fraction of {111} oriented grains parallel to the sample surface, while other samples exhibited nearly random crystallographic texture. The electrochemical results from potentiodynamic polarization and electrochemical impedance spectroscopy showed a decrease in corrosion resistance from 87 µm to 53 µm grain size sample and then an increase for the 26 µm grain size sample. This increase was attributed to the dominant effect of recrystallization texture on the corrosion behavior of the sample. The cathodic hydrogen evolution reaction kinetics was found to play a decisive role in the corrosion behavior of iron.Team Yaiza Gonzalez GarciaTeam Maria Santofimia NavarroTeam Jilt Sietsm

    Predicting the effect of droplet geometry and size distribution on atmospheric corrosion

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    A new approach is proposed to numerically predict and study atmospheric corrosion for ranging droplet size distributions and the influence of the droplet geometry. The proposed methodology allows for a corrosion prediction based on observed droplet size distributions and droplet contact angles. A mechanistic finite element model, including oxygen transport and Butler-Volmer kinetics, is solved in order to obtain the current density as a function of the droplet geometry. This is done for a range of both droplet radii and contact angles. The computed corrosion current densities are then used as input for imposed droplet size distributions. This allows for a calculated material loss estimation for different distributions and electrolyte configurations and shows the extent of the impact of the droplet size distribution on atmospheric corrosion.Green Open Access added to TU Delft Institutional Repository 'You share, we take care!' - Taverne project https://www.openaccess.nl/en/you-share-we-take-care Otherwise as indicated in the copyright section: the publisher is the copyright holder of this work and the author uses the Dutch legislation to make this work public.Team Yaiza Gonzalez GarciaTeam Arjan Mo
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