19 research outputs found
Scale-up of milling in a 100 liter device for processing of TiFeMn alloy for hydrogen storage applications: procedure and characterization
No full textIn this work, the mechanical milling of a FeTiMn alloy for hydrogen storage purposes was performed in an industrial milling device. The TiFe hydride is interesting from the technological standpoint because of the abundance and the low cost of its constituent elements Ti and Fe, as well as its high volumetric hydrogen capacity. However, TiFe is difficult to activate, usually requiring a thermal treatment above 400 °C. A TiFeMn alloy milled for just 10 minutes in a 100 liter industrial milling device showed excellent hydrogen storage properties without any thermal treatment. The as-milled TiFeMn alloy did not need any activation procedure and showed fast kinetic behavior and good cycling stability. Microstructural and morphological characterization of the as-received and as-milled TiFeMn alloys revealed that the material, presents reduced particle and crystallite sizes, even after such short time of milling. The refined microstructure of the as-milled TiFeMn is deemed to account for the improved hydrogen absorption-desorption properties.Fil: Bellosta von Colbe, José. Helmholtz–Zentrum Geesthacht. ; AlemaniaFil: Puszkiel, Julián Atilio. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Comisión Nacional de Energía Atómica; ArgentinaFil: Capurso, Giovanni. Helmholtz–Zentrum Geesthacht. ; AlemaniaFil: Franz, Andreas. ZoZ GmbH; AlemaniaFil: Ulrich Benz, Hans. ZoZ GmbH; AlemaniaFil: Zoz, Henning. ZoZ GmbH; AlemaniaFil: Klassen, Thomas. Helmholtz–Zentrum Geesthacht. ; AlemaniaFil: Dornheim, Martin. Helmholtz–Zentrum Geesthacht. ; Alemani
Transport phenomena versus intrinsic kinetics: Hydrogen sorption limiting sub-process in metal hydride beds
No full textThis paper discusses and compares the different sub-processes that occur during the hydrogen sorption of practical systems based on metal hydrides, i.e. intrinsic kinetics, heat transfer and hydrogen transport. Derived from their modeling equations, a resistance analysis is developed on these hydrogen sorption sub-processes for the first time. This analysis allows quantifying how strongly each sub-process affects the overall sorption kinetics in a hydride bed and thereby the sorption-rate limiting sub-process can be identified. It was found that in the case of the hydrogen absorption of sodium alanate material the heat transfer resistance is the dominant and rate limiting sub-process, with the exception of small geometries. Besides, the resistance due to hydrogen transport is negligible in comparison to the overall absorption resistance. As a consequence, simulations and designs of scaled-up systems based on sodium alanate material always require heat transfer optimization as one of the foremost considerations
Research and development of hydrogen carrier based solutions for hydrogen compression and storage
No full textIndustrial and public interest in hydrogen technologies has risen strongly recently, as hydrogen is the ideal means for medium to long term energy storage, transport and usage in combination with renewable and green energy supply. In a future energy system, the production, storage and usage of green hydrogen is a key technology. Hydrogen is and will in future be even more used for industrial production processes as a reduction agent or for the production of synthetic hydrocarbons, especially in the chemical industry and in refineries. Under certain conditions material based systems for hydrogen storage and compression offer advantages over the classical systems based on gaseous or liquid hydrogen. This includes in particular lower maintenance costs, higher reliability and safety. Hydrogen storage is possible at pressures and temperatures much closer to ambient conditions. Hydrogen compression is possible without any moving parts and only by using waste heat. In this paper, we summarize the newest developments of hydrogen carriers for storage and compression and in addition, give an overview of the different research activities in this field.Full Tex
Materials for hydrogen-based energy storage – past, recent progress and future outlook
No full textGlobally, the accelerating use of renewable energy sources, enabled by increased efficiencies and reduced costs, and driven by the need to mitigate the effects of climate change, has significantly increased research in the areas of renewable energy production, storage, distribution and end-use. Central to this discussion is the use of hydrogen, as a clean, efficient energy vector for energy storage. This review, by experts of Task 32, “Hydrogen-based Energy Storage” of the International Energy Agency, Hydrogen TCP, reports on the development over the last 6 years of hydrogen storage materials, methods and techniques, including electrochemical and thermal storage systems. An overview is given on the background to the various methods, the current state of development and the future prospects. The following areas are covered; porous materials, liquid hydrogen carriers, complex hydrides, intermetallic hydrides, electrochemical storage of energy, thermal energy storage, hydrogen energy systems and an outlook is presented for future prospects and research on hydrogen-based energy storage.Full Tex
+ Reactive Hydride Composite as a Potential Hydrogen Storage Material: Hydrogenation and Dehydrogenation Pathway
No full textA reactive hydride composite (RHC) with initial composition 3CaH(2) + 4MgB(2) + CaF2 was studied by in situ synchrotron radiation powder X-ray diffraction (SR-PXD) and X-ray absorption near edge structure (XANES) at the B K-edge and at the Ca K-edge. The hydrogenation reaction proceeds by an unknown intermediate. No evidence of intermediates was observed during the dehydrogenation reaction. B and Ca K-edge XANES results hint to a closed interaction of CaF2 and Ca(BH4)(2). The main function of CaF2 in the 3CaH(2) + 4MgB(2) + CaF2 RHC is as a dopant for the hydrogenation and dehydrogenation reactions
Hydrogen storage in Mg-LiBH4 composites catalyzed by FeF3
No full textMg-10 mol% LiBH4 composite plus small amounts of FeF3 is investigated in the present work. The presence of LiBH4 during the milling process noticeably modifies the size and morphology of the Mg agglomerates, leading to faster hydrogenation and reaching almost the theoretical hydrogen capacity owing to enhanced hydrogen diffusion mechanism. However, the dehydrogenation of the system at low temperatures (<= 300 degrees C) is still slow. Thus, FeF3 addition is proposed to improve the dehydrogenation kinetic behavior. From experimental results, it is found that the presence of FeF3 results in an additional size reduction of the Mg agglomerates between similar to 10 and similar to 100 mu m and the formation of stable phases such as MgF2, LiF and FeB. The FeB species might have a catalytic effect upon the MgH2 decomposition. As a further result of the FeF3 addition, the Mg-10 mol%LiBH4-5 mol% FeF3 material shows improved dehydrogenation properties: reduced dehydrogenation activation energy, faster hydrogen desorption rate and reversible hydrogen capacities of about 5 wt% at 275 degrees C. (C) 2014 Elsevier B.V. All rights reserved
