Transmission, Distribution & Storage

Recently perovskite-type oxides have attracted researchers as new materials for solid hydrogen storage. This paper presents the performances of perovskite-type oxide LaCrO3 dedicated for hydrogen solid storage using both numerical and experimental methods. Ab initio calculations have been used here with the aim to investigate the electronic mechanical and elastic properties of LaCrO3Hx (x = 0 6) for hydrogen storage applications. Cell parameters crystal structures and mechanical properties are determined. Additionally the cohesive energy indicates the stability of the hydride. Furthermore the mechanical properties showed that both compounds (before and after hydrogenation) are stable. The microstructure and storage capacity at different temperatures of these compounds have been studied. We have shown that storage capacities are around 4 wt%. The properties obtained from this type of hydride showed that it can be used for future applications. XRD analysis was conducted in order to study the structural properties of the compound. Besides morphological thermogravimetric analysis was also conducted on the perovskite-type oxide. Finally a comparison of these materials with other hydrides used for hydrogen storage was carried out.

This work discusses the design and demonstration of an in-situ test setup for testing pipeline steels in a high pressure gaseous hydrogen (H2 ) environment. A miniature hollow pipe-like tensile specimen was designed that acts as the gas containment volume during the test. Specific areas of the specimen can be forced to fracture by selective notching as performed on the weldment. The volume of H2 used was minimised so the test can be performed safely without the need of specialised equipment. The setup is shown to be capable of characterising Hydrogen Embrittlement (HE) in steels through testing an X60 pipeline steel and its weldment. The percentage elongation (%El) of the base metal was found to be reduced by 40% when tested in 100 barg H2 . Reduction of cross-sectional area (%RA) was found to decrease by 28% and 11% in the base metal and weld metal respectively when tested in 100 barg H2 . Benchmark test were performed at 100 barg N2 pressure. SEM fractography further indicated a shift from normal ductile fracture mechanisms to a brittle transgranular (TG) quasi-cleavage (QC) type fracture that is characteristic of HE.

Electrochemical cells and systems play a key role in a wide range of industry sectors. These devices are critical enabling technologies for renewable energy; energy management conservation and storage; pollution control/monitoring; and greenhouse gas reduction. A large number of electrochemical energy technologies have been developed in the past. These systems continue to be optimized in terms of cost life time and performance leading to their continued expansion into existing and emerging market sectors. The more established technologies such as deep-cycle batteries and sensors are being joined by emerging technologies such as fuel cells large format lithium-ion batteries electrochemical reactors; ion transport membranes and supercapacitors. This growing demand (multi-billion dollars) for electrochemical energy systems along with the increasing maturity of a number of technologies is having a significant effect on the global research and development effort which is increasing in both in size and depth. A number of new technologies which will have substantial impact on the environment and the way we produce and utilize energy are under development. This paper presents an overview of several emerging electrochemical energy technologies along with a discussion some of the key technical challenges.

Reinforced concrete (RC) structures are long-term operated objects with service life of 50–100 years. During their operation they subject to continuous ambient effects (cyclic temperature changes acid rains de-icing salts) and service loads (e.g. traffic) which effect on structural integrity of the composite and lead to worsening of structures serviceability. One of the reasons for strength loss of RC members is bond degradation between rebar and concrete. It could be caused by two different factors: overprotection of RC and reinforcement corrosion. These effects were simulated in the laboratory conditions by the electrochemical methods applying of impressed cathodic current and accelerated corrosion tests respectively. It was shown that applied anode polarization causes not only concrete cracking due to internal pressure of corrosion products at the interface but also due to their expansion far from rebar for a distance comparative with a specimen thickness evidently into preliminary formed cracks. Since intensive corrosion of steel reinforcement decreases its diameter and corrosion products can migrate from the rebar surface into a depth of concrete these factors could weaken bond in RC installations up to a total loss of cohesion between rebar and concrete. The influence of cathodic polarization of steel embedded in concrete is commonly seemed to consist in its possible hydrogen embrittlement and ions redistribution in concrete matrix. In this paper the effect of hydrogen recombined at the rebar–concrete interface on bond weakening and concrete cracking is considered.

As the share of distributed renewable power generation increases high electricity prices and low feed-in tariff rates encourage the generation of electricity for personal use. In the building sector this has led to growing interest in energy self-sufficient buildings that feature battery and hydrogen storage capacities. In this study we compare potential technology pathways for residential energy storage in terms of their economic performance by means of a temporal optimization model of the fully self-sufficient energy system of a single-family building taking into account its residential occupancy patterns and thermal equipment. We show for the first time how heat integration with reversible solid oxide cells (rSOCs) and liquid organic hydrogen carriers (LOHCs) in high-efficiency single-family buildings could by 2030 enable the self-sufficient supply of electricity and heat at a yearly premium of 52% against electricity supplied by the grid. Compared to lithium-ion battery systems the total annualized cost of a self-sufficient energy supply can be reduced by 80% through the thermal integration of LOHC reactors and rSOC systems.

For prohibiting a global warming fuel-cell systems without carbon dioxide emissions are a one of the promising technique. In case of a fuel-cell vehicle (FCV) high-pressure H₂ gas is indispensable for a long running range. Although there are lot of paper for studying a hydrogen embrittlement (HE) there are few paper referred to the effect of high-pressure H₂on the HE phenomenon.

In this study an effect of high-pressure H₂ gas on tensile & fatigue properties of stainless steel SUS316L were investigated by means of the internal high-pressure H₂ gas technique. Main findings of this study are as follows;

• Although there are almost no hydrogen embrittlement effect on the 0.2 % proof stress and tensile strength elongation and reduction of area decrease in H₂ gas environment
• For case of low Ni_eq material fatigue life and fatigue limit decrease in H₂ gas environment
• For case of low Ni_eq material not a few α’ martensitic phase generated on the fatigue fractured specimen.

The actual safety margins of gas pipelines depend on a number of factors that include the mechanical characteristics of the material. The evolution with time of the metal properties can be evaluated by mechanical tests performed at different scales seeking for the best compromise between the simplicity of the experimental setup to be potentially employed in situ and the reliability of the results. Possible alternatives are comparatively assessed on pipeline steels of different compositions and in different states.

Formation of metal hydrides is a serious complication that occur when hydride forming metals such as zirconium niobium vanadium and magnesium are exposed to long term hydrogen environment. The main concern is that the hydride as being a brittle material has very poor fracture mechanical properties. Formation of hydride is associated with transportation of hydrogen along the gradients of increasing hydrostatic stress which leads to crack tips and other stress concentrators where it forms the hydride. In the present study the thermodynamics of the evolving hydrides is studied. The process is driven by the release of free strain chemical and gradient energies. A phase field model is used to capture the driving forces that the release of the free energy causes. The study gives the conditions that lead to hydride advancement versus retreat and under which conditions the metal-hydride interface becomes unstable and develops a waviness. The spatial frequency spectrum leading to instability is found to depend on the ratio of the elastic strain energy density and parameters related to the interface energy.

A solid-state storage system is the most practical option for hydrogen because it is more convenient and safer. Metal hydrides especially MgH₂ are the most promising materials that offer high gravimetric capacity and good reversibility. However the practical application of MgH₂ is restricted by slow sorption kinetics and high stability of thermodynamic properties. Hydrogen storage performance of MgH₂ was enhanced by introducing the Mg–Na–Al system that destabilises MgH₂ with NaAlH₄. The Mg–Na–Al system has superior performance compared to that of unary MgH₂ and NaAlH₄. To boost the performance of the Mg–Na–Al system the ball milling method and the addition of a catalyst were introduced. The Mg–Na–Al system resulted in a low onset decomposition temperature superior cyclability and enhanced kinetics performances. The Al12Mg17 and NaMgH₃ that formed in situ during the dehydrogenation process modify the reaction pathway of the Mg–Na–Al system and alter the thermodynamic properties. In this paper the overview of the recent progress in hydrogen storage of the Mg–Na–Al system is detailed. The remaining challenges and future development of Mg–Na–Al system are also discussed. This paper is the first review report on hydrogen storage properties of the Mg–Na–Al system.

Magnesium hydride and selected magnesium-based ternary hydride (Mg2FeH6 Mg2NiH4 and Mg2CoH5) syntheses and modification methods as well as the properties of the obtained materials which are modified mostly by mechanical synthesis or milling are reviewed in this work. The roles of selected additives (oxides halides and intermetallics) nanostructurization polymorphic transformations and cyclic stability are described. Despite the many years of investigations related to these hydrides and the significant number of different additives used there are still many unknown factors that affect their hydrogen storage properties reaction yield and stability. The described compounds seem to be extremely interesting from a theoretical point of view. However their practical application still remains debatable.