215 research outputs found

    Proyecto de implementación de un nuevo sistema de seguimiento de los procesos de industrialización de las piezas de un asiento en un proveedor de primer nivel del sector del automóvil

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    [ES] La homologación de los componentes del sector de la automoción se realiza a través de un proceso largo y complejo denominado Part Approval Production Process (PPAP). La realización del mismo no se puede hacer eficientemente sin un sistema de información adecuado debido a la gran cantidad de información y de fuentes de la misma que se manejan. El alcance global del presente trabajo es implementar una mejora del sistema existente para reducir los retrasos recurrentes en la homologación de los componentes de asientos. En primer lugar, el proyecto tratará de plantear el contexto y las etapas del proceso de homologación de un componente. A continuación, se analizará el sistema que se está usando actualmente y se destacarán las incidencias observadas. Tras haber diseñado los requerimientos que tiene que tener el nuevo sistema, se aprovechará el lanzamiento de un nuevo asiento para implementar un nuevo sistema global que pretende facilitar la ejecución del PPAP y los flujos de información. Un análisis de cumplimiento de requerimientos permitirá detectar las oportunidades de mejora y se concluirá el trabajo con la implementación de dos herramientas proporcionando soluciones a corto plazo para resolver incidencias urgentes.[EN] The approval of automotive parts is being carried out through a complex process called Part Approval Production Process (PPAP). Efficient PPAP completion is impossible without an appropriate information system due to the large quantity of information and information sources that have to be dealt with. The global purpose of present paper is implementing an improvement of an existing system in order to reduce automotive seats components approval delays. First of all, general context and process steps of PPAP will be detailed. Then, the analysis of the current information system will be performed, and its inefficiencies will be pointed out. After having designed the requirements new information system must meet, the kick-off of a new seat will be taken advantage of to implement a new global system that is supposed to enhance PPAP execution and communication flow. Afterwards, to highlight the improvement opportunities, fulfilment of requirements will be analysed, and present work will be concluded with the implementation of two information tools offering short-term solutions able to solve urgent issues.Buriez, E. (2019). Proyecto de implementación de un nuevo sistema de seguimiento de los procesos de industrialización de las piezas de un asiento en un proveedor de primer nivel del sector del automóvil. http://hdl.handle.net/10251/125737TFG

    Electron Transfer Catalysis of The Hydrogenolysis of Acyl Dicarbonyl Cyclopentadienyliron Complexes by Tributyltin Hydride

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    The conversion of acyl dicarbonyl cyclopentadienyliron compounds Cp(CO)2Fe(COR) into aldehydes is not straightforward. It is shown here, mainly from electrochemical results, that the hydrogenolysis of the metal acyl bond can be efficiently achieved by trialkytin hydrides under very mild conditions, according to a chain reaction process initiated by an electron transfer to the acyl complex. The expected aldehyde is formed together with the heterobinuclear iron-tin complex

    Electron Transfer Catalysis of The Hydrogenolysis of Acyl Dicarbonyl Cyclopentadienyliron Complexes by Tributyltin Hydride

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    The conversion of acyl dicarbonyl cyclopentadienyliron compounds Cp(CO)2Fe(COR) into aldehydes is not straightforward. It is shown here, mainly from electrochemical results, that the hydrogenolysis of the metal acyl bond can be efficiently achieved by trialkytin hydrides under very mild conditions, according to a chain reaction process initiated by an electron transfer to the acyl complex. The expected aldehyde is formed together with the heterobinuclear iron-tin complex

    Top-of-Atmosphere Albedo Estimation from Angular Distribution Models Using Scene Identification from Satellite Cloud Property Retrievals

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    International audienceThe next generation of earth radiation budget satellite instruments will routinely merge estimates of global top-of-atmosphere radiative fluxes with cloud properties. This information will offer many new opportunities for validating radiative transfer models and cloud parameterizations in climate models. In this study, five months of Polarization and Directionality of the Earth's Reflectances 670-nm radiance measurements are considered in order to examine how satellite cloud property retrievals can be used to define empirical angular distribution models (ADMs) for estimating top-of-atmosphere albedo. ADMs are defined for 19 scene types defined by satellite retrievals of cloud fraction and cloud optical depth. Two approaches are used to define the ADM scene types. The first assumes there are no biases in the retrieved cloud properties and defines ADMs for fixed discrete intervals of cloud fraction and cloud optical depth (fixed-τ approach). The second approach involves the same cloud fraction intervals, but uses percentile intervals of cloud optical depth instead (percentile-τ approach). Albedos generated using these methods are compared with albedos inferred directly from the mean observed reflectance field

    Electrochemical attachment of a conjugated amino-ferrocifen complex onto carbon and metal surfaces

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    International audienceThe attachment of a pi-conjugated amino-ferrocifen complex was electrochemically achieved either by direct oxidation of the amino group or via the oxidation of the ferrocene moiety. In the first case, the modification consists in oxidizing, at +0.70V/SCE, the amino moiety to its radical cation, which upon deprotonation from the amino group, yields all aminyl radical that may add onto the electrode surface. Alternatively, it is demonstrated that the amine moiety can be indirectly oxidized through an intramolecular electron transfer from the amino moiety to the ferrocenyl group after oxidation of the ferrocene part at +0.40 V. This can occur thanks to the conjugated pi system of the complex. More importantly. it is demonstrated that the covalent attachment of the complex can be achieved on glassy carbon, gold, and platinum surfaces whatever the approach used. The possible mechanisms for the covalent attachment are discussed. Interestingly, it is also shown that the amino-ferrocene compound adsorbs very well likely via pi stacking between grafted and non-grafted molecules. Nevertheless, the adsorbed molecules could be easily removed after passing the electrode in an ultrasonic bath. The electrode coverage was determined under various conditions by integration of the corresponding voltammograms. (C) 2008 Elsevier B.V. All rights reserved

    POLDER observations of cloud bidirectional reflectances compared to a plane-parallel model using the International Satellite Cloud Climatology Project cloud phase functions

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    International audienceThis study investigates the validity of the plane-parallel cloud model and in addition the suitability of water droplet and ice polycrystal phase functions for stratocumulus and cirrus clouds, respectively. To do that, we take advantage of the multidirectional viewing capability of the Polarization and Directionality of the Earth's Reflectances (POLDER) instrument which allows us to characterize the anisotropy of the reflected radiation field. We focus on the analysis of airborne-POLDER data acquired over stratocumulus and cirrus clouds during two selected flights (on April 17 and April 18, 1994) of the European Cloud and Radiation Experiment (EUCREX'94) campaign. The bidirectional reflectances measured in the 0.86 μm channel are compared to plane-parallel cloud simulations computed with the microphysical models used by the International Satellite Cloud Climatology Project (ISCCP). Although clouds are not homogeneous plane-parallel layers, the extended cloud layers under study appear to act, on average, as a homogeneous plane-parallel layer. The standard water droplet model (with an effective radius of 10 μm) used in the ISCCP analysis seems to be suitable for stratocumulus clouds. The relative root-mean-square difference between the observed bidirectional reflectances and the model is only 2%. For cirrus clouds, the water droplet cloud model is definitely inadequate since the rms difference rises to 9%; when the ice polycrystal model chosen for the reanalysis of ISCCP data is used instead, the rms difference is reduced to 3%

    The replacement of a phenol group by an aniline or acetanilide group enhances the cytotoxicity of 2-ferrocenyl-1,1-diphenyl-but-1-ene compounds against breast cancer cells

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    International audienceWe have previously shown that conjugated ferrocenyl p-phenols show strong cytotoxic effects against both the hormone-dependent MCF-7 and hormone-independent MDA-MB-231 breast cancer cell lines, possibly via oxidative quinone methide formation. We now present a series of analogous amine and acetamide compounds: 2-ferrocenyl-1-(4-aminophenyl)-1-phenyl-but-1-ene (Z+E-2), 2-ferrocenyl-1-(4-N-acetylaminophenyl)-1-phenyl-but-1-ene (Z-3), and their corresponding organic molecules 1-(4-aminophenyl)-1,2-bis-phenyl-but-1-ene (Z+E-4) and 1-(4-N-acetamidophenyl)-1,2-bis-phenyl-but-1-ene (Z+E-5). All of the compounds have adequate relative binding affinity values for the estrogen receptor; between 2.8% and 5.7% for ERα, and between 0.18% and 15.5% for ERβ, as well as exothermic ligand binding in in silico ER docking experiments. Compounds 2 and 3 show dual estrogenic/cytotoxic activity on the MCF-7 cell line; they are proliferative at low concentrations (0.1 μM) and antiproliferative at high concentrations (10 μM). On the MDA-MB-231 cell line, the ferrocenyl complexes 2 and 3 are antiproliferative with IC50 values of 0.8 μM for 2 and 0.65 μM for 3, while the purely organic molecules 4 and 5 show no effect. Electrochemical experiments suggest that both 2 and 3 can be transformed to oxidized quinoid-type species, analogous to what had previously been observed for the ferrocene phenols
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