Long-Term Stability of Thin-Film Pd-Based Supported Membranes

Membrane reactors have demonstrated a large potential for the production of hydrogen via reforming of different feedstocks in comparison with other reactor types. However, the long-term performance and stability of the applied membranes are extremely important for the possible industrial exploitation of these reactors. This study investigates the long-term stability of thin-film Pd-Ag membranes supported on porous Al2O3 supports. The stability of five similarly prepared membranes have been investigated for 2650 h, up to 600 °C and in fluidized bed conditions. Results show the importance and the contribution of the sealing of the membranes at temperatures up to 500 °C. At higher temperatures the membranes surface deformation results in pinhole formation and a consequent decrease in selectivity. Stable operation of the membranes in a fluidized bed is observed up to 450 °C, however, at higher temperatures the scouring action of the particles under fluidization causes significant deformation of the palladium surface resulting in a decreased selectivity.The presented work is funded within BIONICO. This project has received funding from the Fuel Cells and Hydrogen 2 Joint Undertaking under grant agreement No 671459. This Joint Undertaking receives support from the European Union’s Horizon 2020 Research and Innovation Programme, Hydrogen Europe and N.ERGHY

Mixed Ionic-Electronic Conducting Membranes (MIEC) for Their Application in Membrane Reactors: A Review

Mixed ionic-electronic conducting membranes have seen significant progress over the last 25 years as efficient ways to obtain oxygen separation from air and for their integration in chemical production systems where pure oxygen in small amounts is needed. Perovskite materials are the most employed materials for membrane preparation. However, they have poor phase stability and are prone to poisoning when subjected to CO2 and SO2, which limits their industrial application. To solve this, the so-called dual-phase membranes are attracting greater attention. In this review, recent advances on self-supported and supported oxygen membranes and factors that affect the oxygen permeation and membrane stability are presented. Possible ways for further improvements that can be pursued to increase the oxygen permeation rate are also indicated. Lastly, an overview of the most relevant examples of membrane reactors in which oxygen membranes have been integrated are provided.This project has received funding from the European Union’s Horizon 2020 research and innovation programme under grant agreement No 679933. The present publication reflects only the author’s views and the European Union is not liable for any use that may be made of the information contained therein

Recent Advances in Pd-Based Membranes for Membrane Reactors

Palladium-based membranes for hydrogen separation have been studied by several research groups during the last 40 years. Much effort has been dedicated to improving the hydrogen flux of these membranes employing different alloys, supports, deposition/production techniques, etc. High flux and cheap membranes, yet stable at different operating conditions are required for their exploitation at industrial scale. The integration of membranes in multifunctional reactors (membrane reactors) poses additional demands on the membranes as interactions at different levels between the catalyst and the membrane surface can occur. Particularly, when employing the membranes in fluidized bed reactors, the selective layer should be resistant to or protected against erosion. In this review we will also describe a novel kind of membranes, the pore-filled type membranes prepared by Pacheco Tanaka and coworkers that represent a possible solution to integrate thin selective membranes into membrane reactors while protecting the selective layer. This work is focused on recent advances on metallic supports, materials used as an intermetallic diffusion layer when metallic supports are used and the most recent advances on Pd-based composite membranes. Particular attention is paid to improvements on sulfur resistance of Pd based membranes, resistance to hydrogen embrittlement and stability at high temperature.The presented work is funded within Reforcell (grant agreement No. 278997) and FERRET (grant agreement No. 621181) projects as part of European Union's Seventh Framework Programme (FP7/2007-2013) for the Fuel Cells and Hydrogen Joint Technology Initiative

Ultra-pure hydrogen production via ammonia decomposition in a catalytic membrane reactor

In this work two alternatives are presented for increasing the purity of hydrogen produced in a membrane reactor for ammonia decomposition. It is experimentally demonstrated that either increasing the thickness of the membrane selective layer or using a small purification unit in the permeate of the membranes, ultra-pure hydrogen can be produced. Specifically, the results show that increasing the membrane thickness above 6 μm ultra-pure hydrogen can be obtained at pressures below 5 bar. A cheaper solution, however, consists in the use of an adsorption bed downstream the membrane reactor. In this way, ultra-pure hydrogen can be achieved with higher reactor pressures, lower temperatures and thinner membranes, which result in lower reactor costs. A possible process diagram is also reported showing that the regeneration of the adsorption bed can be done by exploiting the heat available in the system and thus introducing no additional heat sources.This project receives support from the European Union’s Horizon 2020 research and nnovation under grant agreement No. 862482 (ARENHA project)

Achievements of European projects on membrane reactor for hydrogen production

Membrane reactors for hydrogen production can increase both the hydrogen production efficiency at small scale and the electric efficiency in micro-cogeneration systems when coupled with Polymeric Electrolyte Membrane fuel cells. This paper discusses the achievements of three European projects (FERRET, FluidCELL, BIONICO) which investigate the application of the membrane reactor concept to hydrogen production and micro-cogeneration systems using both natural gas and biofuels (biogas and bio-ethanol) as feedstock. The membranes, used to selectively separate hydrogen from the other reaction products (CH4, CO2, H2O, etc.), are of asymmetric type with a thin layer of Pd alloy (<5 μm), and supported on a ceramic porous material to increase their mechanical stability. In FERRET, the flexibility of the membrane reactor under diverse natural gas quality is validated. The reactor is integrated in a micro-CHP system and achieves a net electric efficiency of about 42% (8% points higher than the reference case). In FluidCELL, the use of bio-ethanol as feedstock for micro-cogeneration Polymeric Electrolyte Membrane based system is investigated in off-grid applications and a net electric efficiency around 40% is obtained (6% higher than the reference case). Finally, BIONICO investigates the hydrogen production from biogas. While BIONICO has just started, FERRET and FluidCELL are in their third year and the two prototypes are close to be tested confirming the potentiality of membrane reactor technology at small scale.The research leading to these results has received funding from the Fuel Cells and Hydrogen Joint Technology Initiative under grant agreements No 621181 (FERRET), No 621196 (FluidCELL). BIONICO has received funding from the Fuel Cells and Hydrogen 2 Joint Undertaking under grant agreement No 671459. This Joint Undertaking receives support from the European Union's Horizon 2020 research and innovation programme, Hydrogen Europe and N.ERGHY

Kinetic model for Pd-based membranes coking/deactivation in propane dehydrogenation processes

This work aims at providing insight into the deactivation mechanism of Pd-based membranes in propane dehydrogenation processes. Thermogravimetric analysis (TGA) experiments were conducted to study the adsorption and coking of propylene over conventional thin layer (TL) and double-skinned (DS) Pd-based membranes under several operating conditions. A mechanistic monolayer-multilayer coke growth model was selected to mathematically describe the membrane coking observed during TGA experiments. In addition, the reaction rate of coke formation and its influence on membranes deactivation has been studied. The deactivation model able to describe the hydrogen flux decay over time suggests that monolayer coke is the main responsible for the membrane deactivation. Multilayer coke also causes deactivation but with a smaller order than monolayer coke, for both the TL and the DS membranes. Among the two membrane types, DS membrane deactivates faster, i.e. with a higher order than the TL membrane, which is equal to 1.55 for the former and 0.51 for the latter. This is related to the higher number of active sites available in the controlling step of the deactivation reaction, which are most probably given by the addition of the ceramic Al2O3 protective layer. XPS spectra further confirms that, in the presence of Pd, Al2O3 sites contribute to carbon formation by evidencing a different nature of carbon formed on the two membranes. Finally, the experimental results of hydrogen permeation over time conducted on different membranes types and operative conditions confirmed the validity of the derived and parametrized kinetic models for coke formation and membrane deactivation. The experimental findings and the kinetic model derived in this work provide essential tools for the design and optimization of membrane reactors for dehydrogenation processes.This project has received funding from the European Union’s Horizon 2020 research and innovation program under grant agreement No 814671 (BiZeolCat)

Unravelling the transport mechanism of pore-filled membranes for hydrogen separation

The permeation characteristics of palladium pore filled (PF) membranes have been investigated with gas permeation and structural characterization of the membranes. PF membranes have been prepared by filling with Pd the nanoporous γ-Al2O3/YSZ (or pure YSZ) layer supported onto porous α-Al2O3 and ZrO2. The number of nanoporous layers and the applied vacuum level during the electroless plating process have been studied. Gas permeation properties of the PF membranes have been determined in a temperature range of 300-550 °C. The measured hydrogen permeances have been found to be lower than previously reported for similar membranes. It has been found that the hydrogen fluxes do not depend on the thickness of the nanoporous layers (γ-Al2O3/YSZ or pure YSZ) or on the vacuum pump employed for filling with Pd. The physicochemical characterization performed showed that the palladium deposited does not form a percolated network across the mesoporous layer(s), leading to low hydrogen permeances and thus low H2/N2 perm-selectivities.The presented work is funded within FERRET project as part of European Union’s Seventh Framework Programme (FP7/2007-2013) for the Fuel Cells and Hydrogen Joint Technology Initiative under grant agreement n° 621181. The Talos TEM was funded as part of HEFCE funding in the UK Research Partnership Investment Funding (UKRPIF) Manchester RPIF Round 2

Attrition-resistant membranes for fluidized-bed membrane reactors: Double-skin membranes

Pd-Ag supported membranes have been prepared by coating a ceramic interdiffusion barrier onto a Hastelloy X (0.2 µm media grade) porous support followed by deposition of the hydrogen selective Pd-Ag (4–5 µm) layer by electroless plating. To one of the membranes an additional porous Al2O3-YSZ layer (protective layer with 50 wt% of YSZ) was deposited by dip-coating followed by calcination at 550 °C on top of the Pd-Ag layer, and this membrane is referred to as a double-skin membrane. Both membranes were integrated at the same time in a single reactor in order to assess and compare the performance of both membranes under identical conditions. The membranes have first been tested in an empty reactor with pure gases (H2 and N2) and afterwards in the presence of a catalyst (rhodium onto promoted alumina) fluidized in the bubbling regime. The membranes immersed in the bubbling bed were tested at 400 °C and 500 °C for 115 and 500 h, respectively. The effect of the protective layer on the permeation properties and stability of the membranes were studied. The double-skinned membraned showed a H2 permeance of 1.55·10−6 mol m−2 s−1 Pa−1 at 500 °C and 4 bar of pressure difference with an ideal perm-selectivity virtually infinite before incorporation of particles. This selectivity did not decay during the long term test under fluidization with catalyst particles.The presented work is funded within FERRET project as part of European Union's Seventh Framework Programme (FP7/2007-2013) for the Fuel Cells and Hydrogen Joint Technology Initiative under grant agreement n. 621181. Note: “The present publication reflects only the authors' views and the Union is not liable for any use that may be made of the information contained therein”

Regeneration of Exhausted Palladium-Based Membranes: Recycling Process and Economics

The aim of the present work is the recycling treatment of tubular α-Al2O3-supported ceramic membranes with a Pd/Ag selective layer, employed in hydrogen production with integrated CO2 capture. A nitric acid leaching treatment was investigated, and recovered ceramic supports were characterized, demonstrating their suitability for the production of novel efficient membranes. The main objective was the metal dissolution that preserved the support integrity in order to allow the recovered membrane to be suitable for a new deposition of the selective layer. The conditions that obtained a satisfactory dissolution rate of the Pd/Ag layer while avoiding the support to be damaged are as follows: nitric acid 3 M, 60 °C and 3.5 h of reaction time. The efficiency of the recovered supports was determined by nitrogen permeance and surface roughness analysis, and the economic figures were analysed to evaluate the convenience of the regeneration process and the advantage of a recycled membrane over a new membrane. The experimentation carried out demonstrates the proposed process feasibility both in terms of recycling and economic results.This research has received funding from the European Union’s Horizon 2020 research and innovation programme under grant agreement no. 760944 (MEMBER project)

Preparación y caracterización de recubrimientos de DLC (Diamond-Like Carbon) mediante deposición química en fase vapor asistida por plasma

El objetivo principal del presente proyecto ha consistido en la preparación y caracterización de recubrimientos de carbono cuasi diamante DLC (Diamond-Like Carbon) mediante la técnica de deposición química en fase vapor asistida por plasma (Plasma Enhanced Chemical Vapor Deposition, PECVD), empleando para ello una fuente de voltaje bias pulsada bipolar asimétrica para la polarización del substrato, y metano como gas precursor. Con el fin de mejorar la adherencia de los recubrimientos sobre substratos de acero, se doparon los recubrimientos con diferentes concentraciones de silicio a partir de la introducción de tetrametilsilano (TMS). Los recubrimientos depositados han de presentar buenas propiedades mecánicas y tribológicas (elevada dureza y bajo coeficiente de fricción) además de una buena adherencia. La composición química y estructural de los recubrimientos se estudió mediante espectroscopía Raman visible y espectroscopía fotoelectrónica de rayos X (XPS). La morfología en sección de los recubrimientos, así como los espesores obtenidos fueros analizados por microscopía electrónica de barrido (SEM) y microscopía óptica confocal. La dureza se caracterizó por medio de la técnica de nanoindentación. El coeficiente de fricción y la adherencia de los recubrimientos se analizaron mediante la realización de ensayos de microrayado. Los recubrimientos DLC obtenidos presentaron una estructura con un contenido en enlaces sp3 del 30 %, con una dureza aproximada de 20 GPa y un coeficiente de fricción inferior a 0,1. Los recubrimientos dopados con silicio presentaron menores valores de dureza (13-18 GPa) y sus coeficientes de fricción llegaron a valores inferiores a 0,05. La adherencia de los recubrimientos dopados con silicio mejoró con respecto a la de los recubrimientos sin dopar