Browsing by Author "Melendez, J."
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Item Direct route from ethanol to pure hydrogen through autothermal reforming in a membrane reactor: Experimental demonstration, reactor modelling and design: Experimental demonstration, reactor modelling and design(2018-01-15) Spallina, V.; Matturro, G.; Ruocco, C.; Meloni, E.; Palma, V.; Fernández-Gesalaga, E.; Melendez, J.; Pacheco Tanaka, David A.; Viviente Sole, J.L.; van Sint Annaland, M.; Gallucci, F.; Tecnalia Research & Innovation; TECNOLOGÍAS DE HIDRÓGENO; TECNOLOGÍA DE MEMBRANAS E INTENSIFICACIÓN DE PROCESOSThis work reports the integration of thin (∼3–4 μm thick) Pd-based membranes for H2 separation in a fluidized bed catalytic reactor for ethanol auto-thermal reforming. The performance of a fluidized bed membrane reactor has been investigated from an experimental and numerical point of view. The demonstration of the technology has been carried out over 50 h under reactive conditions using 5 thin Pd-based alumina-supported membranes and a 3 wt%Pt-10 wt%Ni catalyst deposited on a mixed CeO2/SiO2 support. The results have confirmed the feasibility of the concept, in particular the capacity to reach a hydrogen recovery factor up to 70%, while the operation at different fluidization regimes, oxygen-to-ethanol and steam-to-ethanol ratios, feed pressures and reactor temperatures have been studied. The most critical part of the system is the sealing of the membranes, where most of the gas leakage was detected. A fluidized bed membrane reactor model for ethanol reforming has been developed and validated with the obtained experimental results. The model has been subsequently used to design a small reactor unit for domestic use, showing that 0.45 m2 membrane area is needed to produce the amount of H2 required for a 5 kWe PEM fuel-cell based micro-CHP system.Item The membrane-assisted chemical looping reforming concept for efficient H2 production with inherent CO2 capture: Experimental demonstration and model validation: Experimental demonstration and model validation(2018-04-01) Medrano, J.A.; Potdar, I.; Melendez, J.; Spallina, V.; Pacheco Tanaka, David A.; van Sint Annaland, M.; Gallucci, F.; Tecnalia Research & Innovation; TECNOLOGÍA DE MEMBRANAS E INTENSIFICACIÓN DE PROCESOSIn this work a novel reactor concept referred to as Membrane-Assisted Chemical Looping Reforming (MA-CLR) has been demonstrated at lab scale under different operating conditions for a total working time of about 100 h. This reactor combines the advantages of Chemical Looping, such as CO2 capture and good thermal integration, with membrane technology for a better process integration and direct product separation in a single unit, which in its turn leads to increased efficiencies and important benefits compared to conventional technologies for H2 production. The effect of different operating conditions (i.e. temperature, steam-to-carbon ratio or oxygen feed in the reactor) has been evaluated in a continuous chemical looping reactor, and methane conversions above 90% have been measured with (ultra-pure) hydrogen recovery from the membranes. For all the cases a maximum recovery factor of around 30% has been measured, which could be increased by operating the concept at higher pressures and with more membranes. The optimum conditions have been found at temperatures around 600 °C for a steam-to-carbon ratio of 3 and diluted air in the air reactor (5% O2). The complete demonstration has been carried out feeding up to 1 L/min of CH4 (corresponding to 0.6 kW of thermal input) while up to 1.15 L/min of H2 was recovered. Simultaneously, a phenomenological model has been developed and validated with the experimental results. In general, good agreement is observed, with overall deviations below 10% in terms of methane conversion, H2 recovery and separation factor. The model allows better understanding of the behavior of the MA-CLR concept and the optimization and design of scaled-up versions of the concept.Item Preparation and characterization of thin-film Pd-Ag supported membranes for high-temperature applications(2015-10-19) Fernandez, E.; Coenen, K.; Helmi, A.; Melendez, J.; Zuñiga, J.; Pacheco Tanaka, D. A.; Van Sint Annaland, M.; Gallucci, F.; TECNOLOGÍAS DE HIDRÓGENO; Tecnalia Research & Innovation; TECNOLOGÍA DE MEMBRANAS E INTENSIFICACIÓN DE PROCESOSThis paper reports the preparation, characterization and stability tests of thin-film Pd-Ag supported membranes for high-temperature fluidized bed membrane reactor applications. Various thin-film supported membranes have been prepared by simultaneous Pd-Ag electroless plating and have been initially sealed with a sealing procedure previously validated for Water gas shift (WGS) application (400 °C). The membranes have been characterized for single gas and mixed gas permeation, and for methane steam and autothermal reforming in a fluidized bed membrane reactor at 550-600 °C using a Ru-based catalyst. In addition, the performance of these membranes was compared to commercial membranes from REB Research & Consulting under the same reaction conditions. The applied sealing showed nitrogen leaks at 600 °C and different sealing approaches were tested solving this problem. Finally, also the long-term stability of the thin-film Pd-Ag supported membrane at 600 °C has been investigated.