Publications

As the transport sector is ought to be decarbonized fuel-cell-powered trains are a viable zero-tailpipe technology alternative to the widely employed diesel multiple units in regional railway service on non-electrified tracks. Carbon-free hydrogen can be provided by water-electrolysis from renewable energies. In this study we introduce an approach to assess the potential of wind-based hydrogen for use in adjacent regional rail transport by applying a GIS approach in conjunction with a site-level cost model. In Brandenburg about 10.1 million train-km annually could be switched to fuel cell electric train operation. This relates to a diesel consumption of appr. 9.5 million liters today. If fuel cell trains would be employed that translated to 2198 annual tons hydrogen annually. At favorable sites hydrogen costs of approx. 6.40 €/kg - including costs of hydrogen refueling stations - could be achieved. Making excess hydrogen available for other consumers would further decrease hydrogen production costs.

The recent advances on the effects of microstructural refinement and various nano-catalytic additives on the hydrogen storage properties of metal and complex hydrides obtained in the last few years in the allied laboratories at the University of Waterloo (Canada) and Military University of Technology (Warsaw Poland) are critically reviewed in this paper. The research results indicate that microstructural refinement (particle and grain size) induced by ball milling influences quite modestly the hydrogen storage properties of simple metal and complex metal hydrides. On the other hand the addition of nanometric elemental metals acting as potent catalysts and/or metal halide catalytic precursors brings about profound improvements in the hydrogen absorption/desorption kinetics for simple metal and complex metal hydrides alike. In general catalytic precursors react with the hydride matrix forming a metal salt and free nanometric or amorphous elemental metals/intermetallics which in turn act catalytically. However these catalysts change only kinetic properties i.e. the hydrogen absorption/desorption rate but they do not change thermodynamics (e.g. enthalpy change of hydrogen sorption reactions). It is shown that a complex metal hydride LiAlH4 after high energy ball milling with a nanometric Ni metal catalyst and/or MnCl2 catalytic precursor is able to desorb relatively large quantities of hydrogen at RT 40 and 80 °C. This kind of behavior is very encouraging for the future development of solid state hydrogen systems.

Climate change is one of the most serious threats to the human habitat. The required structural change to limit anthropogenic forcing is expected to fundamentally change daily social and economic life. The production of iron and steel is a special case of economic activities since it is not only associated with combustion but particularly with process emissions of greenhouse gases which have to be dealt with likewise. Traditional mitigation options of the sector like efficiency measures substitution with less emission-intensive materials or scrap-based production are bounded and thus insufficient for rapid decarbonization necessary for complying with long-term climate policy targets. Iron and steel products are basic materials at the core of modern socio-economic systems additionally being essential also for other mitigation options like hydro and wind power. Therefore a system-wide assessment of recent technological developments enabling almost complete decarbonization of the sector is substantially relevant. Deploying a recursive-dynamic multi-region multi-sector computable general equilibrium approach we investigate switches from coke-to hydrogen-based iron and steel technologies in a scenario framework where industry decisions (technological choice and timing) and climate policies are mis-aligned. Overall we find that the costs of industry transition are moderate but still ones that may represent a barrier for implementation because the generation deciding on low-carbon technologies and bearing (macro)economic costs might not be the generation benefitting from it. Our macroeconomic assessment further indicates that anticipated bottom-up estimates of required additional domestic renewable electricity tend to be overestimated. Relative price changes in the economy induce electricity substitution effects and trigger increased electricity imports. Sectoral carbon leakage is an imminent risk and calls for aligned course of action of private and public actors.

The growing rate of electricity generation from renewables is leading to new operational and management issues on the power grid because the electricity generated exceeds local requirements and the transportation or storage capacities are inadequate. An interesting option that is under investigation by several years is the opportunity to use the renewable electricity surplus to power electrolyzers that split water into its component parts with the hydrogen being directly injected into natural gas pipelines for both storage and transportation. This innovative approach merges together the concepts of (i) renewable power-to-hydrogen (P2H) and of (ii) hydrogen blending into natural gas networks. The combination of renewable P2H and hydrogen blending into natural gas networks has a huge potential in terms of environmental and social benefits but it is still facing several barriers that are technological economic legislative. In the framework of the new hydrogen strategy for a climate-neutral Europe Member States should design a roadmap moving towards a hydrogen ecosystem by 2050. The blending of “green hydrogen” that is hydrogen produced by renewable sources in the natural gas network at a limited percentage is a key element to enable hydrogen production in a preliminary and transitional phase. Therefore it is urgent to evaluate at the same time (i) the potential of green hydrogen blending at low percentage (up to 10%) and (ii) the maximum P2H capacity compatible with low percentage blending. The paper aims to preliminary assess the green hydrogen blending potential into the Italian natural gas network as a tool for policy makers grid and networks managers and energy planners.

Pipeline failure caused by Hydrogen-Induced Cracking (HIC) also known as Hydrogen Embrittlement (HE) is a pressing issue for the oil and natural gas industry. Bursts in pipelines are devastating and extremely costly. The explosive force of a bursting pipe can inflict fatal injuries to workers while the combined loss of product and effort to repair are highly costly to producers. Further pipeline failures due to HIC have a long lasting impact on the surrounding environment. Safe use and operation of such pipelines depend on a good understanding of the underlying forces that cause HIC. Specifically a reliable way to predict the growth rate of hydrogen-induced cracks is needed to establish a safe duration of service for each length of pipeline. Pipes that have exceeded or are near the end of their service life can then be retired before the risk of HIC-related failures becomes too high. However little is known about the mechanisms that drive HIC. To date no model has been put forth that accurately predicts the growth rate of fractures due to HIC under extreme pressures such as in the context of natural gas and petroleum pipelines. Herein a mathematical model for the growth of fractures by HIC under extreme pressures is presented. This model is derived from first principles and the results are compared with other models. The implications of these findings are discussed and a description of future work based on these findings is presented.

The aim of this study was to validate a model for predicting overpressure arising from accidental hydrogen releases in areas with limited ventilation. Experiments were performed in a large-scale setup that included a steel-reinforced container of volume 14.9 m³ and variable ventilation areas and mass flow rates. The pressure peaking phenomenon characterized as transient overpressure with a characteristic peak in a vented enclosure was observed during all the experiments. The model description presented the relationship between the ventilation area mass flow rate enclosure volume and discharge coefficient. The experimental results were compared with two prediction models representing a perfect mix and the real mix. The perfect mix assumed that all the released hydrogen was well stirred inside the enclosure during the releases. The real mix prediction s used the hydrogen concentration and temperature data measured during experiments. The prediction results with both perfect mix and real mix showed possible hazards during unignited hydrogen releases.

With the rapid growth in demand for effective and renewable energy the hydrogen era has begun. To meet commercial requirements efficient hydrogen storage techniques are required. So far four techniques have been suggested for hydrogen storage: compressed storage hydrogen liquefaction chemical absorption and physical adsorption. Currently high-pressure compressed tanks are used in the industry; however certain limitations such as high costs safety concerns undesirable amounts of occupied space and low storage capacities are still challenges. Physical hydrogen adsorption is one of the most promising techniques; it uses porous adsorbents which have material benefits such as low costs high storage densities and fast charging–discharging kinetics. During adsorption on material surfaces hydrogen molecules weakly adsorb at the surface of adsorbents via long-range dispersion forces. The largest challenge in the hydrogen era is the development of progressive materials for efficient hydrogen storage. In designing efficient adsorbents understanding interfacial interactions between hydrogen molecules and porous material surfaces is important. In this review we briefly summarize a hydrogen storage technique based on US DOE classifications and examine hydrogen storage targets for feasible commercialization. We also address recent trends in the development of hydrogen storage materials. Lastly we propose spillover mechanisms for efficient hydrogen storage using solid-state adsorbents.

Recently hydrogen (H2) has emerged as a superior energy carrier that has the potential to replace fossil fuel. However storing H2 under safe and operable conditions is still a challenging process due to the current commercial method i.e. H2 storage in a pressurised and liquified state which requires extremely high pressure and extremely low temperature. To solve this problem re‐ search on solid‐state H2 storage materials is being actively conducted. Among the solid‐state H2 storage materials borohydride is a potential candidate for H2 storage owing to its high gravimetric capacity (majority borohydride materials release >10 wt% of H2). Mg(BH4)2 which is included in the borohydride family shows promise as a good H2 storage material owing to its high gravimetric capacity (14.9 wt%). However its practical application is hindered by high thermal decomposition temperature (above 300 °C) slow sorption kinetics and poor reversibility. Currently the general research on the use of additives to enhance the H2 storage performance of Mg(BH4)2 is still under investigation. This article reviews the latest research on additive‐enhanced Mg(BH4)2 and its impact on the H2 storage performance. The future prospect and challenges in the development of additive‐ enhanced Mg(BH4)2 are also discussed in this review paper. To the best of our knowledge this is the first systematic review paper that focuses on the additive‐enhanced Mg(BH4)2 for solid‐state H2 storage.

The Small Punch test has been recently used to estimate mechanical properties of steels in aggressive environments. This technique very interesting when there is shortage of material consists in using a small plane specimen and punch it until it fails. The type of tests normally used are under a constant load in an aggressive environment with the target to determine the threshold stress. However this is an inaccurate technique which takes time as the tests are quite slow. In this paper the Small Punch tests are combined with the step loading technique collected in the standard ASTM F1624 [1] to obtain the value of threshold stress of an S420 steel in a total time of approximately one week. The ASTM F1624 indicates how to apply constant load steps in hydrogen embrittlement environments increasing them subsequently and adapting their duration until the specimen fails. The environment is created by means of cathodic polarization of cylindrical tensile specimens in an acid electrolyte. A batch of standard tests are performed to validate the methodology.

Hydrogen energy is a possible solution for storage in the future. The resistance of packaging materials such as stainless steels has to be guaranteed for a possible use of these materials as containers for highly pressurized hydrogen. The effect of hydrogen charging on the nucleation and growth of microdamage in two different austenitic stainless steels AISI316 and AISI316L was studied using in situ tensile tests in synchrotron X-ray tomography. Information about damage nucleation void growth and void shape were obtained. AISI316 was found to be more sensitive to hydrogen compared to AISI316L in terms of ductility loss. It was measured that void nucleation and growth are not affected by hydrogen charging. The effect of hydrogen was however found to change the morphology of nucleated voids from spherical cavities to micro-cracks being oriented perpendicular to the tensile axis.