37 resultados para Pequeña producción


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El presente proyecto consiste en el análisis y búsqueda de soluciones para el control de producción de la unidad de rodajes de la compañía CAF S.A. Para ello, se ha tenido que analizar procesos de producción, capturar requerimientos, desarrollar unas herramientas de control de producción temporales y elaborar una especificación de requisitos. Sin olvidar la gestión e interlocución con proveedores. Estas líneas de trabajo se encuentran descritas en esta memoria, junto con análisis de resultados, conclusiones y unas líneas futuras donde se seguirá trabajando.

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1000 p. (Anexos: 929-965 p.; bibliografía 965-1000 p.). Capítulos de discusión y conclusiones en castellano y francés.

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[ES]El presente trabajo consiste en el análisis exergético de una planta experimental con microcogeneración diseñada para satisfacer la demanda de agua caliente sanitaria de un bloque de viviendas. El ACS la generan una caldera con producción de energía térmica variable y una unidad de microcogneración que produce 5 kW eléctricos y 12 kW térmicos. El análisis exergético que se realiza en el trabajo permite determinar la eficiencia del uso que se hace del combustible, y compararla con la de una planta convencional.

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[ES]La energía solar fotovoltaica es un sistema de generación eléctrica cada vez más importante entre los países desarrollados. En este contexto, España siempre ha sido una de los países que más ha invertido a lo largo de su historia. En los últimos años, sin embargo, por culpa del déficit tarifario esta situación ha cambiado, implantando medidas para ahorrar costes que a largo plazo deterioran dicho sector. En el trabajo, se presenta un estudio que muestra la actualidad de este tejido empresarial. Para ello, se ha realizado una encuesta a varias empresas, sobre la situación del sector y las perspectivas de crecimiento y desarrollo dentro de ese entorno. Así, se ha concluido con algunas de las consecuencias que pueden suceder debido al cambio de legislación.

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En este trabajo se va a explicar la relación que existe entre la optimización de un problema lineal y el problema dual correspondiente. Se usara la herramienta Solver del Microsoft Excel para resolver los el problema de programación lineal planteado. Se analizaran los resultados obtenidos tanto del problema primal como del problema dual y se explicara el significado de los resultados obtenidos. Se finalizara con unas conclusiones donde se expondría lo aprendido durante este trabajo y el significado económico de este tipo de problemas.

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El cultivo de hongos comestibles saprófitos constituye un sistema de producción-consumo, que ha adquirido gran relevancia social, económica y ecológica. Con el fin de abaratar costes a la vez que aprovechar y reciclar residuos forestales, el objetivo de este trabajo se ha centrado en evaluar la viabilidad del aserrín de Eucalyptus globulus como soporte del cultivo en bolsa de Lentinula edodes (hongo comercializado conocido como Shiitake) y Agrocybe aegerita (hongo no comercializado comúnmente llamado Seta de Chopo). Se han evaluado 6 formulaciones, todas ellas con el aserrín como componente principal y con adición de diferentes suplementos: cereales (salvado y mijo), un controlador del pH (CaCO3) y un estimulador de crecimiento (CaSO4). Se ha determinado el crecimiento miceliar sobre cada uno de los sustratos, así como la producción de carpoforos (tanto en cantidad como en calidad) y la duración del periodo de fructificación. La mezcla más efectiva para la producción de L. edodes fue aquella que contenía yeso y azúcar mientras que para A. aegerita el salvado resultó ser el mejor suplemento.

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El consumo acelerado de unos recursos energéticos finitos, el impacto ambiental asociado a la producción y uso de las energías tradicionales, la distribución de las reservas de energía , y los precios de las materias primas energéticas , confieren a las fuentes renovables de energía una importancia creciente en la política energética de la mayor í a de los países desarrollados. Además , la valorizació n energética de residuos representa un reto de la sociedad de consumo, por una parte para dar respuest a a los requerimientos de desarrollo sostenible y tamb ié n para fomentar el uso de fuentes de energí a renovables. Entre estos, una de las fuente s más importantes es la biomasa. Es evidente que, un desarrollo de las tecnologías y una planificación adecuada de los aprovechamientos de biomasa, permitiría contrarrestar los efectos perniciosos del excesivo uso de la energía , además de generar empleo, mejoras ambientales y el correspondiente desarrollo rural de zonas degradadas. Las previsiones establec en que antes de 2100 la cuota de participación de la biomasa en la producción mundial de energía debería estar entre el 25 y el 46 %. La producción de hidró geno a partir de biomasa es un proceso interesante y viable, teniendo en cuenta el aumento significa tivo del actual consumo de hidró geno. La producción actual se obtiene mayoritariamente a partir de fuentes fósiles , que emiten grandes cantidades de CO 2 y por lo tanto, surge la necesidad de reducir estas emisiones utilizando materias primas renovables. Por ello, en este sentido, el objetivo principal de este Proyecto Fin de Grado es avanzar en el aprovechamiento de la biomasa vegetal a través de la piró lisis flash y posterior reformado con vapor en línea para la obtención de hidró geno. Para ello, se ha p ropuesto una primera e tapa de piró lisis rápida a 500 º C en un reactor spouted bed cónico y una segunda etapa catal í tica de r eformado con vapor en lí nea en un lecho fluidizado, con el fin de optimizar la temperatura y el tiempo espacial de la segunda etapa

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Los plásticos proporcionan claros beneficios a la sociedad, es un material de innegable utilidad presente en infinidad de productos de uso cotidiano . No obstante, p ese a no ser considerados resi duos peligrosos, los res i duos plásticos representan un problema ambiental global de creciente preocupación ya que la cultura del uso y desecho que prevalece hoy en día hac e que la generación de res i duos ocurra de manera masiva y conti nua . Además, e l plástico es un material inorgánico que tiene alta durabilidad. Se calcula que puede tardar entre 100 y 1000 años en degradarse d ependiendo del tipo de plástico, lo que supone que no se reincorpore fácilmente a los ciclos naturales, permaneciendo por largos periodos y afectando de diferentes maneras los lugares donde queda dispuesto. Por lo tanto, los impactos ambientales son acumulativos, de largo plazo y lejanos. El interés de reciclar los plá sticos surge por la necesidad de eliminar su dep ó sito en vertederos, donde dada su baja degradabilidad solo originan problemas medioambientales y de deterioro del paisaje. A nivel mundial , el principal impacto ambiental de los res i duos p lásticos es la contaminación de los océanos y mares. Es un impacto acumulativo que se presenta a largo plazo y cubre gran cantidad de espacios de todo el planeta. Se han encontrado cantidades substanciales de residuos contaminando los hábitats marinos desde los polos hasta el ecuador, desde costas remotas inhabitadas hasta costas altamente pobladas y áreas profundas del océano (Barnes y cols., 2009 ) . El bajo peso del plástico, que es una ventaja en las etapas de distri bución y consumo del producto plástico, se convierte en una problemática ambiental cuando los residuos plásticos navegan por corrientes subterráneas, ríos, mares y océanos.

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El objetivo que persigue la línea de investigación en la que se engloba este trabajo es la obtención de hidrógeno desde disoluciones acuosas de metanol (aproximadamente del 10% de metanol), considerando estos compuestos como una forma de almacenar hidrógeno y obtenerlo a baja temperatura “on-board” en un vehículo mediante el reformado en fase acuosa. El reto es conseguir un sistema catalítico de pequeño volumen y rápida respuesta a las demandas de hidrógeno con elevado rendimiento y calidad apropiada (<10 ppm de CO) para las pilas de combustible PEM. Los objetivos planteados en el siguiente trabajo se centran en la preparación y caracterización de un catalizador de platino soportado en alúmina, y la puesta en marcha de un reactor discontinuo de mezcla perfecta a presión para la evaluación de catalizadores en el proceso de reformado en fase líquida.

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Desarrollo de modelos cinéticos para las reacciones de hidrodesulfuración del líquido de pirólisis de neumáticos.

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Investigación realizada dentro del Programa de Formación y Perfeccionamiento de Personal Investigador del Gobierno Vasco (2010-2013).

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[EN] This PhD work started in March 2010 with the support of the University of the Basque Country (UPV/EHU) under the program named “Formación de Personal Investigador” at the Chemical and Environmental Engineering Department in the Faculty of Engineering of Bilbao. The major part of the Thesis work was carried out in the mentioned department, as a member of the Sustainable Process Engineering (SuPrEn) research group. In addition, this PhD Thesis includes the research work developed during a period of 6 months at the Institut für Mikrotechnik Mainz GmbH, IMM, in Germany. During the four years of the Thesis, conventional and microreactor systems were tested for several feedstocks renewable and non-renewable, gases and liquids through several reforming processes in order to produce hydrogen. For this purpose, new catalytic formulations which showed high activity, selectivity and stability were design. As a consequence, the PhD work performed allowed the publication of seven scientific articles in peer-reviewed journals. This PhD Thesis is divided into the following six chapters described below. The opportunity of this work is established on the basis of the transition period needed for moving from a petroleum based energy system to a renewable based new one. Consequently, the present global energy scenario was detailed in Chapter 1, and the role of hydrogen as a real alternative in the future energy system was justified based on several outlooks. Therefore, renewable and non-renewable hydrogen production routes were presented, explaining the corresponding benefits and drawbacks. Then, the raw materials used in this Thesis work were described and the most important issues regarding the processes and the characteristics of the catalytic formulations were explained. The introduction chapter finishes by introducing the concepts of decentralized production and process intensification with the use of microreactors. In addition, a small description of these innovative reaction systems and the benefits that entailed their use were also mentioned. In Chapter 2 the main objectives of this Thesis work are summarized. The development of advanced reaction systems for hydrogen rich mixtures production is the main objective. In addition, the use and comparison between two different reaction systems, (fixed bed reactor (FBR) and microreactor), the processing of renewable raw materials, the development of new, active, selective and stable catalytic formulations, and the optimization of the operating conditions were also established as additional partial objectives. Methane and natural gas (NG) steam reforming experimental results obtained when operated with microreactor and FBR systems are presented in Chapter 3. For these experiments nickel-based (Ni/Al2O3 and Ni/MgO) and noble metal-based (Pd/Al2O3 and Pt/Al2O3) catalysts were prepared by wet impregnation and their catalytic activity was measured at several temperatures, from 973 to 1073 K, different S/C ratios, from 1.0 to 2.0, and atmospheric pressure. The Weight Hourly Space Velocity (WHSV) was maintained constant in order to compare the catalytic activity in both reaction systems. The results obtained showed a better performance of the catalysts operating in microreactors. The Ni/MgO catalyst reached the highest hydrogen production yield at 1073 K and steam-to-carbon ratio (S/C) of 1.5 under Steam methane Reforming (SMR) conditions. In addition, this catalyst also showed good activity and stability under NG reforming at S/C=1.0 and 2.0. The Ni/Al2O3 catalyst also showed high activity and good stability and it was the catalyst reaching the highest methane conversion (72.9 %) and H2out/CH4in ratio (2.4) under SMR conditions at 1073 K and S/C=1.0. However, this catalyst suffered from deactivation when it was tested under NG reforming conditions. Regarding the activity measurements carried out with the noble metal-based catalysts in the microreactor systems, they suffered a very quick deactivation, probably because of the effects attributed to carbon deposition, which was detected by Scanning Electron Microscope (SEM). When the FBR was used no catalytic activity was measured with the catalysts under investigation, probably because they were operated at the same WHSV than the microreactors and these WHSVs were too high for FBR system. In Chapter 4 biogas reforming processes were studied. This chapter starts with an introduction explaining the properties of the biogas and the main production routes. Then, the experimental procedure carried out is detailed giving concrete information about the experimental set-up, defining the parameters measured, specifying the characteristics of the reactors used and describing the characterization techniques utilized. Each following section describes the results obtained from activity testing with the different catalysts prepared, which is subsequently summarized: Section 4.3: Biogas reforming processes using γ-Al2O3 based catalysts The activity results obtained by several Ni-based catalysts and a bimetallic Rh-Ni catalyst supported on magnesia or alumina modified with oxides like CeO2 and ZrO2 are presented in this section. In addition, an alumina-based commercial catalyst was tested in order to compare the activity results measured. Four different biogas reforming processes were studied using a FBR: dry reforming (DR), biogas steam reforming (BSR), biogas oxidative reforming (BOR) and tri-reforming (TR). For the BSR process different steam to carbon ratios (S/C) from 1.0 to 3.0, were tested. In the case of BOR process the oxygen-to-methane (O2/CH4) ratio was varied from 0.125 to 0.50. Finally, for TR processes different S/C ratios from 1.0 to 3.0, and O2/CH4 ratios of 0.25 and 0.50 were studied. Then, the catalysts which achieved high activity and stability were impregnated in a microreactor to explore the viability of process intensification. The operation with microreactors was carried out under the best experimental conditions measured in the FBR. In addition, the physicochemical characterization of the fresh and spent catalysts was carried out by Inductively Coupled Plasma Atomic Emission Spectroscopy (ICP-AES), N2 physisorption, H2 chemisorption, Temperature Programmed Reduction (TPR), SEM, X-ray Photoelectron Spectroscopy (XPS) and X-ray powder Diffraction (XRD). Operating with the FBR, conversions close to the ones predicted by thermodynamic calculations were obtained by most of the catalysts tested. The Rh-Ni/Ce-Al2O3 catalyst obtained the highest hydrogen production yield in DR. In BSR process, the Ni/Ce-Al2O3 catalyst achieved the best activity results operating at S/C=1.0. In the case of BOR process, the Ni/Ce-Zr-Al2O3 catalyst showed the highest reactants conversion values operating at O2/CH4=0.25. Finally, in the TR process the Rh-Ni/Ce-Al2O3 catalyst obtained the best results operating at S/C=1.0 and O2/CH4=0.25. Therefore, these three catalysts were selected to be coated onto microchannels in order to test its performance under BOR and TR processes conditions. Although the operation using microreactors was carried out under considerably higher WHSV, similar conversions and yields as the ones measured in FBR were measured. Furthermore, attending to other measurements like Turnover Frequency (TOF) and Hydrogen Productivity (PROD), the values calculated for the catalysts tested in microreactors were one order of magnitude higher. Thus, due to the low dispersion degree measured by H2-chemisorption, the Ni/Ce-Al2O3 catalyst reached the highest TOF and PROD values. Section 4.4: Biogas reforming processes using Zeolites L based catalysts In this section three type of L zeolites, with different morphology and size, were synthesized and used as catalyst support. Then, for each type of L zeolite three nickel monometallic and their homologous Rh-Ni bimetallic catalysts were prepared by the wetness impregnation method. These catalysts were tested using the FBR under DR process and different conditions of BSR (S/C ratio of 1.0 and 2.0), BOR (O2/CH4 ratio of 0.25 and 0.50) and TR processes (at S/C=1.0 and O2/CH4=0.25). The characterization of these catalysts was also carried out by using the same techniques mentioned in the previous section. Very high methane and carbon dioxide conversion values were measured for almost all the catalysts under investigation. The experimental results evidenced the better catalytic behavior of the bimetallic catalysts as compared to the monometallic ones. Comparing the catalysts behavior with regards to their morphology, for the BSR process the Disc catalysts were the most active ones at the lowest S/C ratio tested. On the contrary, the Cylindrical (30–60 nm) catalysts were more active under BOR conditions at O2/CH4=0.25 and TR processes. By the contrary, the Cylindrical (1–3 µm) catalysts showed the worst activity results for both processes. Section 4.5: Biogas reforming processes using Na+ and Cs+ doped Zeolites LTL based catalysts A method for the synthesis of Linde Type L (LTL) zeolite under microwave-assisted hydrothermal conditions and its behavior as a support for heterogeneously catalyzed hydrogen production is described in this section. Then, rhodium and nickel-based bimetallic catalysts were prepared in order to be tested by DR process and BOR process at O2/CH4=0.25. Moreover, the characterization of the catalysts under investigation was also carried out. Higher activities were achieved by the catalysts prepared from the non-doped zeolites, Rh-Ni/D and Rh-Ni/N, as compared to the ones supported on Na+ and Cs+ exchanged supports. However, the differences between them were not very significant. In addition, the Na+ and Cs+ incorporation affected mainly to the Disc catalysts. Comparing the results obtained by these catalysts with the ones studied in the section 4.4, in general worst results were achieved under DR conditions and almost the same results when operated under BOR conditions. In Chapter 5 the ethylene glycol (EG) as feed for syngas production by steam reforming (SR) and oxidative steam reforming (OSR) was studied by using microchannel reactors. The product composition was determined at a S/C of 4.0, reaction temperatures between 625°C and 725°C, atmospheric pressure and Volume Hourly Space Velocities (VHSV) between 100 and 300 NL/(gcath). This work was divided in two sections. The first one corresponds to the introduction of the main and most promising EG production routes. Then, the new experimental procedure is detailed and the information about the experimental set-up and the measured parameters is described. The characterization was carried out using the same techniques as for the previous chapter. Then, the next sections correspond to the catalytic activity and catalysts characterization results. Section 5.3: xRh-cm and xRh-np catalysts for ethylene glycol reforming Initially, catalysts with different rhodium loading, from 1.0 to 5.0 wt. %, and supported on α-Al2O3 were prepared by two different preparation methods (conventional impregnation and separate nanoparticle synthesis). Then, the catalysts were compared regarding their measured activity and selectivity, as well as the characterization results obtained before and after the activity tests carried out. The samples prepared by a conventional impregnation method showed generally higher activity compared to catalysts prepared from Rh nanoparticles. By-product formation of species such as acetaldehyde, ethane and ethylene was detected, regardless if oxygen was added to the feed or not. Among the catalysts tested, the 2.5Rh-cm catalyst was considered the best one. Section 5.4: 2.5Rh-cm catalyst support modification with CeO2 and La2O3 In this part of the Chapter 5, the catalyst showing the best performance in the previous section, the 2.5Rh-Al2O3 catalyst, was selected in order to be improved. Therefore, new Rh based catalysts were designed using α-Al2O3 and being modified this support with different contents of CeO2 or La2O3 oxides. All the catalysts containing additives showed complete conversion and selectivities close to the equilibrium in both SR and OSR processes. In addition, for these catalysts the concentrations measured for the C2H4, CH4, CH3CHO and C2H6 by-products were very low. Finally, the 2.5Rh-20Ce catalyst was selected according to its catalytic activity and characterization results in order to run a stability test, which lasted more than 115 hours under stable operation. The last chapter, Chapter 6, summarizes the main conclusions achieved throughout this Thesis work. Although very high reactant conversions and rich hydrogen mixtures were obtained using a fixed bed reaction system, the use of microreactors improves the key issues, heat and mass transfer limitations, through which the reforming reactions are intensified. Therefore, they seem to be a very interesting and promising alternative for process intensification and decentralized production for remote application.

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En este trabajo analizo cuáles son los supuestos epistemológicos y ontológicos de las recientes Leyes 3/2007 y 14/2012 en torno a la identidad de género y la transexualidad y cómo éstas forman parte del conjunto de dispositivos de poder y control tecno-biopolítico sobre las vidas de las personas. Comienzo por un recorrido teórico sobre la construcción de la categoría de sexo y género, continúo con los derechos sobre identidad de género y orientación sexual reconocidos a nivel internacional, trazo algunas de las distintas posturas y reivindicaciones de los movimientos sociales, después hago un breve recorrido por distintas normativas en torno al género en el Estado Español desde 1931 y finalmente termino con un análisis de las leyes española 3/2007 y la vasca 14/2012.

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El objeto del proyecto es el diseño de un molde para la fabricación en serie de una pieza de plástico, concretamente, el componente exterior de la rejilla del radiador de un nuevo modelo de vehículo automóvil de próximo lanzamiento perteneciente al modelo de la compañía “Toyota”.