Transmission, Distribution & Storage

Without remorse fossil fuels have made a huge contribution to global development in all of its forms. However the recent scientific outlooks are currently shifting as more research is targeted towards promoting a carbon-free economy in addition to the use of electric power from renewable sources. While renewable energy sources may be a solution to the anthropogenic greenhouse gas (GHG) emissions from fossil fuel they are yet season-dependent faced with major atmospheric drawbacks which when combined with annually varying but steady energy demand results in renewable energy excesses or deficits. Therefore it is essential to devise a long-term storage medium to balance their intermittent demand and supply. Hydrogen (H2) as an energy vector has been suggested as a viable method of achieving the objectives of meeting the increasing global energy demand. However successful implementation of a full-scale H2 economy requires large-scale H2 storage (as H2 is highly compressible). As such storage of H2 in geological formations has been considered as a potential solution where it can be withdrawn again at the larger stage for utilization. Thus in this review we focus on the potential use of geological formations for large-scale underground hydrogen storage (UHS) where both conventional and non-conventional UHS options were examined in depth. Also insights into some of the probable sites and the related examined criteria for selection were highlighted. The hydrodynamics of UHS influencing factors (including solid fluid and solid–fluid interactions) are summarized exclusively. In addition the economics and reaction perspectives inherent to UHS have been examined. The findings of this study show that UHS like other storage systems is still in its infancy. Further research and development are needed to address the significant hurdles and research gaps found particularly in replaceable influencing parameters. As a result this study is a valuable resource for UHS researchers.

Hydrogen sulfide corrosion is one of the main reasons of steels destruction in the oil and gas industry. Damages appear as a result of corrosion and hydrogen embrittlement and corrosion cracking occurs when the load is applied. The influence of the steels structure on its stress corrosion cracking under the loads in hydrogen sulfide environment is insufficiently studied. The aim of the study is to determine the influence of the steels structure on its corrosion hydrogenation and corrosion cracking in the NACE hydrogen sulfide solution.<br/>It was established that the corrosion rate and hydrogenation of steel У8 in the NACE solution grows when the structure dispersion increases from perlite to sorbite troostite and martensite. The corrosion rate and hydrogenation of steel 45 are the greatest in pearlite-ferrite while the smallest - in sorbite.<br/>The corrosion of steels У8 and 45 in the NACE solution is localized: the average size of the ulcers is 50 ... 80 μm on the steel У8 and 45 ... 65 μm on steel 45. The depth of ulcers is maximal on the steel У8 with the martensite structure (~ 260 μm) and on the steel 45 with the troostite structure (~ 210 μm).<br/>Static load (σ = 300 MPa) increases the hydrogenation of steels in the hydrogen sulfide environment. The concentration of hydrogen in steel У8 with troostite structure increases by ~ 1.8 times. The concentration of hydrogen in steel 45 with troostite and martensite structures increases by ~ 1.2...1.3 and by ~ 1.4...1.6 times respectively.<br/>The steel У8 with martensite and perlite structures and steel 45 with troostite structure has the lowest resistance to corrosion cracking. Steels destruction depends on both hydrogen permeation and the corrosion localization which leads to the increase of the microelectrochemical heterogeneity of the surfaces.

Fundamental understanding of H localization in steel is an important step towards theoretical descriptions of hydrogen embrittlement mechanisms at the atomic level. In this paper we investigate the interaction between atomic H and defects in ferromagnetic body-centered cubic (bcc) iron using density functional theory (DFT) calculations. Hydrogen trapping profiles in the bulk lattice at vacancies dislocations and grain boundaries (GBs) are calculated and used to evaluate the concentrations of H at these defects as a function of temperature. The results on H-trapping at GBs enable further investigating H-enhanced decohesion at GBs in Fe. A hierarchy map of trapping energies associated with the most common crystal lattice defects is presented and the most attractive H-trapping sites are identified.

The problem of anthropogenically driven climate change and its inextricable link to our global society’s present and future energy needs are arguably the greatest challenge facing our planet. Hydrogen is now widely regarded as one key element of a potential energy solution for the twenty-first century capable of assisting in issues of environmental emissions sustainability and energy security. Hydrogen has the potential to provide for energy in transportation distributed heat and power generation and energy storage systems with little or no impact on the environment both locally and globally. However any transition from a carbon-based (fossil fuel) energy system to a hydrogen-based economy involves significant scientific technological and socio-economic barriers. This brief report aims to outline the basis of the growing worldwide interest in hydrogen energy and examines some of the important issues relating to the future development of hydrogen as an energy vector.



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Mechanical properties of metals and their alloys are most often determined by interstitial atoms. Hydrogen as one common interstitial element is often found to degrade the fracture behavior and lead to premature or catastrophic failure in a wide range of materials known as hydrogen embrittlement. This topic has been studied for more than a century yet the basic mechanisms of such degradation remain in dispute for many metallic systems. This work attempts to link experimentally and theoretically between failure caused by the presence of hydrogen and second phases lattice distortion and deformation levels.

This study reports the investigative conclusions of parametric studies conducted to understand the effect of operating parameters on absorption and desorption characteristics of LaNi4.7Al0.3 metal hydride system for thermal management applications. Reactor with improved design containing 55 embedded cooling tubes is fabricated and filled with 4 kg of metal hydride alloy. Using water as heat transfer fluid (HTF) effects of supply pressure HTF temperature and HTF flow rate on absorption and desorption characteristics of the reactor are analyzed. Increasing supply pressure leads to prominent improvement in absorption capacity while the increase in HTF temperature enhanced desorption performance. At 20 bar and 20 °C 46.2877 g of hydrogen (1.16 wt%) was absorbed resulting in total energy output of 707.3 kJ for 300 s. During desorption at 80 °C with water flow rate of 8 lpm heat input of 608.1 kJ for 300 s resulted in 28.5259 g of hydrogen desorption.

Titanium-based alloys are susceptible to hydrogen embrittlement (HE) a phenomenon that deteriorates fatigue properties. Ti-6Al-4V is the most widely used titanium alloy and the effect of hydrogen embrittlement on fatigue crack growth (FCG) was investigated by carrying out crack propagation tests in air and high-pressure H₂ environment. The FCG test in hydrogen environment resulted in a drastic increase in crack growth rate at a certain Δ K with crack propagation rates up to 13 times higher than those observed in air. Possible reasons for such behaviour were discussed in this paper. The relationship between FCG results in high-pressure H₂ environment and microstructure was investigated by comparison with already published results of cast and forged Ti-6Al-4V. Coarser microstructure was found to be more sensitive to HE. Moreover the electron beam melting (EBM) materials experienced a crack growth acceleration in-between that of cast and wrought Ti-6Al-4V

Hydrogen embrittlement is one of the largest obstacles against the commercialisation of ultra-high strength quenching and partitioning (Q&P) steels with ultimate tensile strength over 1500 MPa including the hot stamped steel parts that have undergone a Q&P treatment. In this work the influence of partitioning temperature on hydrogen embrittlement of ultra-high strength Q&P steels is studied by pre-charged tensile tests with both dog-bone and notched samples. It is found that hydrogen embrittlement resistance is enhanced by the higher partitioning temperature. Then the hydrogen embrittlement mechanism is analysed in terms of hydrogen retained austenite and martensite matrix. Thermal desorption analysis (TDA) shows that the hydrogen trapping properties are similar in the Q&P steels which cannot explain the enhancement of hydrogen embrittlement resistance. On the contrary it is found that the relatively low retained austenite stability after the higher temperature partitioning ensures more sufficient TRIP effect before hydrogen-induced fracture. Additionally dislocation recovery and solute carbon depletion at the higher partitioning temperature can reduce the flow stress of the martensite matrix improving its intrinsic toughness and reducing its hydrogen sensitivity both of which result in the higher hydrogen embrittlement resistance.

To limit global warming and mitigate climate change the global economy needs to decarbonize and reduce emissions to net-zero by mid-century. The asymmetries of the global energy system necessitate the deployment of a suite of decarbonization technologies and an all-of-the-above approach to deliver the steep CO₂ -emissions reductions necessary. Carbon capture and storage (CCS) technologies that capture CO₂ from industrial and power-plant point sources as well as the ambient air and store them underground are largely seen as needed to address both the flow of emissions being released and the stock of CO₂ already in the atmosphere. Despite the pressing need to commercialize the technologies their large-scale deployment has been slow. Initial deployment however could lead to near-term cost reduction and technology proliferation and lowering of the overall system cost of decarbonization. As of November 2019 more than half of global large-scale CCS facilities are in the USA thanks to a history of sustained government support for the technologies. Recently the USA has seen a raft of new developments on the policy and project side signalling a reinvigorated push to commercialize the technology. Analysing these recent developments using a policy-priorities framework for CCS commercialization developed by the Global CCS Institute the paper assesses the USA’s position to lead large-scale deployment of CCS technologies to commercialization. It concludes that the USA is in a prime position due to the political economic characteristics of its energy economy resource wealth and innovation-driven manufacturing sector.

Hydrogen was doped in austenitic stainless steel (ASS) 316L tensile samples produced by the laser-powder bed fusion (L-PBF) technique. For this aim an electrochemical method was conducted under a high current density of 100 mA/cm2 for three days to examine its sustainability under extreme hydrogen environments at ambient temperatures. The chemical composition of the starting powders contained a high amount of Ni approximately 12.9 wt.% as a strong austenite stabilizer. The tensile tests disclosed that hydrogen charging caused a minor reduction in the elongation to failure (approximately 3.5% on average) and ultimate tensile strength (UTS; approximately 2.1% on average) of the samples using a low strain rate of 1.2 × 10⁻⁴ s⁻¹. It was also found that an increase in the strain rate from 1.2 × 10⁻⁴ s⁻¹ o 4.8 ×10⁻⁴ s⁻¹ led to a reduction of approximately 3.6% on average for the elongation to failure and 1.7% on average for UTS in the pre-charged samples. No trace of martensite was detected in the X-ray diffraction (XRD) analysis of the fractured samples thanks to the high Ni content which caused a minor reduction in UTS × uniform elongation (UE) (GPa%) after the H charging. Considerable surface tearing was observed for the pre-charged sample after the tensile deformation. Additionally some cracks were observed to be independent of the melt pool boundaries indicating that such boundaries cannot necessarily act as a suitable area for the crack propagation.

To avoid failures due to hydrogen embrittlement it is important to know the amount of hydrogen absorbed by certain steel grades under service conditions. When a critical hydrogen content is reached the material properties begin to deteriorate. The hydrogen uptake and embrittlement of three different carbon steels (API 5CT L80 Type 1 P110 and 42CrMo4) was investigated in autoclave tests with hydrogen gas (H₂) at elevated pressure and in ambient pressure tests with hydrogen sulfide (H₂S). H₂ gas with a pressure of up to 100 bar resulted in an overall low but still detectable hydrogen absorption which did not cause any substantial hydrogen embrittlement in specimens under a constant load of 90% of the specified minimum yield strength (SMYS). The amount of hydrogen absorbed under conditions with H₂S was approximately one order of magnitude larger than under conditions with H₂ gas. The high hydrogen content led to failures of the 42CrMo4 and P110 specimens.

Hydrogen is a notoriously difficult substance to store yet has endless energy applications. Thus the study of long-term hydrogen storage and high-pressure bulk hydrogen storage have been the subject of much research in the last several years. To create a research path forward it is important to know what research has already been done and what is already known about hydrogen storage. In this review several approaches to hydrogen storage are addressed including high-pressure storage cryogenic liquid hydrogen storage and metal hydride absorption. Challenges and advantages are offered based on reported research findings. Since the project looks closely at advanced manufacturing techniques for the same are outlined as well. There are seven main categories into which most rapid prototyping styles fall. Each is briefly explained and illustrated as well as some generally accepted advantages and drawbacks to each style. An overview of hydrogen adsorption on metal hydrides carbon fibers and carbon nanotubes are presented. The hydrogen storage capacities of these materials are discussed as well as the differing conditions in which the adsorption was performed under. Concepts regarding storage shape and materials accompanied by smaller-scale advanced manufacturing options for hydrogen storage are also presented.

The current energy system is subject to a fundamental transformation: A system that is oriented towards a constant energy supply by means of fossil fuels is now expected to integrate increasing amounts of renewable energy to achieve overall a more sustainable energy supply. The challenges arising from this paradigm shift are currently most obvious in the area of electric power supply. However it affects all areas of the energy system albeit with different results. Within the energy system various independent grids fulfill the function of transporting and spatially distributing energy or energy carriers and the demand-oriented supply ensures that energy demands are met at all times. However renewable energy sources generally supply their energy independently from any specific energy demand. Their contribution to the overall energy system is expected to increase significantly.<br/>Energy storage technologies are one option for temporal matching of energy supply and demand. Energy storage systems have the ability to take up a certain amount of energy store it in a storage medium for a suitable period of time and release it in a controlled manner after a certain time delay. Energy storage systems can also be constructed as process chains by combining unit operations each of which cover different aspects of these functions. Large-scale mechanical storage of electric power is currently almost exclusively achieved by pumped-storage hydroelectric power stations.<br/>These systems may be supplemented in the future by compressed-air energy storage and possibly air separation plants. In the area of electrochemical storage various technologies are currently in various stages of research development and demonstration of their suitability for large-scale electrical energy storage. Thermal energy storage technologies are based on the storage of sensible heat exploitation of phase transitions adsorption/desorption processes and chemical reactions. The latter offer the possibility of permanent and loss-free storage of heat. The storage of energy in chemical bonds involves compounds that can act as energy carriers or as chemical feedstocks. Thus they are in direct economic competition with established (fossil fuel) supply routes. The key technology here – now and for the foreseeable future – is the electrolysis of water to produce hydrogen and oxygen.<br/>Hydrogen can be transformed by various processes into other energy carriers which can be exploited in different sectors of the energy system and/or as raw materials for energy-intensive industrial processes. Some functions of energy storage systems can be taken over by industrial processes. Within the overall energy system chemical energy storage technologies open up opportunities to link and interweave the various energy streams and sectors. Chemical energy storage not only offers means for greater integration of renewable energy outside the electric power sector it also creates new opportunities for increased flexibility novel synergies and additional optimization.<br/>Several examples of specific energy utilization are discussed and evaluated with respect to energy storage applications. The article describes various technologies for energy storage and their potential applications in the context of Germany’s Energiewende i.e. the transition towards a more sustainable energy system. Therefore the existing legal framework defines some of the discussions and findings within the article specifically the compensation for renewable electricity providers defined by the German Renewable Energy Sources Act which is under constant reformation. While the article is written from a German perspective the authors hope this article will be of general interest for anyone working in the areas of energy systems or energy technology.

The formation of elongated zirconium hydride platelets during corrosion of nuclear fuel clad is linked to its premature failure due to embrittlement and delayed hydride cracking. Despite their importance however most existing models of hydride nucleation and growth in Zr alloys are phenomenological and lack sufficient physical detail to become predictive under the variety of conditions found in nuclear reactors during operation. Moreover most models ignore the dynamic nature of clad oxidation which requires that hydrogen transport and precipitation be considered in a scenario where the oxide layer is continuously growing at the expense of the metal substrate. In this paper we perform simulations of hydride formation in Zr clads with a moving oxide/metal boundary using a stochastic kinetic diffusion/reaction model parameterized with state-of-the-art defect and solute energetics. Our model uses the solutions of the hydrogen diffusion problem across an increasingly-coarse oxide layer to define boundary conditions for the kinetic simulations of hydrogen penetration precipitation and dissolution in the metal clad. Our method captures the spatial dependence of the problem by discretizing all spatial derivatives using a stochastic finite difference scheme. Our results include hydride number densities and size distributions along the radial coordinate of the clad for the first 1.6 h of evolution providing a quantitative picture of hydride incipient nucleation and growth under clad service conditions.

This paper analyzes the behavior of residential solar-powered electrical energy storage systems. For this purpose a simulation model based on MATLAB/Simulink is developed. Investigating both short-time and seasonal hydrogen-based storage systems simulations on the basis of real weather data are processed on a timescale of 15 min for a consideration period of 3 years. A sensitivity analysis is conducted in order to identify the most important system parameters concerning the proportion of consumption and the degree of self-sufficiency. Therefore the influences of storage capacity and of storage efficiencies are discussed. A short-time storage system can increase the proportion of consumption by up to 35 percentage points compared to a self-consumption system without storage. However the seasonal storing system uses almost the entire energy produced by the photovoltaic (PV) system (nearly 100% self-consumption). Thereby the energy drawn from the grid can be reduced and a degree of self-sufficiency of about 90% is achieved. Based on these findings some scenarios to reach self-sufficiency are analyzed. The results show that full self-sufficiency will be possible with a seasonal hydrogen-based storage system if PV area and initial storage level are appropriate.

Correlating hydrogen embrittlement phenomenon with the metallic microstructural features holds the key for developing metals resistant to hydrogen-based failures. In case of fatigue failure of hydrogen charged metals in addition to the hydrogen-based failure mechanisms associated with monotonic loading such as HELP HEDE etc. microstructural features such as grain size type of grain boundary (special/random) fraction of special grain boundaries; their network and triple junctions can play a complex role. The probable sites for fatigue crack initiation in such metals can be identified as the sites of highest hydrogen concentration or accumulated plastic strain. To this end we have developed an experimental framework based on in-situ fatigue crack initiation and propagation studies under scanning electron microscope (SEM) to identify the weakest link in the metallic microstructure leading to failure. In-situ fatigue experiments are performed on carefully designed polycrystalline nickel (99.95% pure) specimens (miniaturised shallow-notched & electro-polished) using a 10 kN fatigue stage inside the SEM. Electron Back Scattering Diffraction (EBSD) map of the notched region surface helps identify the distribution of special/random grain boundaries triple junctions and grain orientation. The specimen surface in the shallow notched region for both the hydrogen charged and un-charged specimens are then carefully studied to correlate the microstructural feature associated with fatigue crack initiation sites. Such correlation of the fatigue crack initiation site and microstructural feature is further corroborated with the knowledge of hydrogen trapping and grain’s elastic anisotropicity to be either the site of high hydrogen concentration accumulated plastic slip or both.

Development of technologically and economically feasible solutions for hydrogen storage stimulates progress in hydrogen economy. High gravimetric and volumetric capacities of magnesium hydride makes it promising material capable to accelerate implementation of hydrogen-based technologies in our daily life. However widely discussed limitations of sorption kinetics and thermodynamic properties must be managed in MgH2. This work investigates two steps hydrogenation when process of hydrogen absorption is followed after hydrogen plasma activation. Such technique initiates creation of new channels for enhanced hydrogen sorption. Moreover synthesis of negligible amount of hydride acts as positive factor for further hydrogenation.

In this paper we analyze the potential factors affecting the hydrogen sulfide type of stress corrosion cracking in C110 casing pipes. In order to further study these cracking factors the methods of material property testing scanning electron microscopy XRD TEM and 3D ultra-depth-of-field were applied in the experiments. Besides that an HTHP autoclave was independently designed by the laboratory to simulate the actual corrosion environment and the potential factors affecting the stress corrosion cracking of C110 casing pipes were determined. The test results showed that the chemical composition metallographic structure hardness and non-metallic inclusions of the two types of C110 casing pipes were all qualified. In fact there remains a risk of stress corrosion cracking when the two kinds of C110 casing pipes serve under long-term field-working conditions. It is considered in this paper that the precipitates on the material surface stress damage and pitting corrosion are all critical factors affecting the stress corrosion cracking of casing pipes.

The deterioration of the mechanical properties of metal induced by hydrogen absorption threatens the safety of the equipment serviced in hydrogen environments. In this study the hydrogen concentration distribution in 2.25Cr-1Mo-0.25V steel after hydrogen charging was analyzed following the hydrogen permeation and diffusion model. The diffusible hydrogen content in the 1-mm-thick specimen and its influence on the mechanical properties of the material were investigated by glycerol gas collecting test static hydrogen charging tensile test scanning electron microscopy (SEM) test and microhardness test. The results indicate that the content of diffusible hydrogen tends to be the saturation state when the hydrogen charging time reaches 48 h. The simulation results suggest that the hydrogen concentration distribution can be effectively simulated by ABAQUS and the method can be used to analyze the hydrogen concentration in the material with complex structures or containing multiple microstructures. The influence of hydrogen on the mechanical properties is that the elongation of this material is reduced and the diffusible hydrogen will cause a decrease in the fracture toughness of the material and thus hydrogen embrittlement (HE) will occur. Moreover the Young’s modulus E and microhardness are increased due to hydrogen absorption and the variation value is related to the hydrogen concentration introduced into the specimen.

The effect of hydrogen atoms at grain boundaries in metals is usually detrimental to the cohesion of the interface. This effect can be quantified in terms of the strengthening energy which is obtained following the thermodynamic model of Rice and Wang. A critical component of this model is the bonding or solution energy of the atoms to the free surfaces that are created during decohesion. At a grain boundary in a multicomponent system it is not immediately clear how the different species would partition and distribute on the cleaved free surfaces. In this work it is demonstrated that the choice of partitioning pattern has a significant effect on the predicted influence of H and C on grain boundary cohesion. To this end the Σ3(112)[11¯0] symmetric tilt grain boundary in bcc Fe with different contents of interstitial C and H was studied taking into account all possible distributions of the elements as well as surface diffusion effects. H as a single element has a negative influence on grain boundary cohesion independent of the details of the H distribution. C on the other hand can act both ways enhancing or reducing the cohesion of the interface. The effect of mixed H and C compositions depends on the partition pattern. However the general trend is that the number of detrimental cases increases with increasing H content. A decomposition of the strengthening energy into chemical and mechanical contributions shows that the elastic contribution dominates at high C contents while the chemical contribution sets the trend for high H contents.

When steel components fail in service due to the intervention of hydrogen assisted cracking discussion of the root cause arises. The failure is frequently blamed on component design working conditions the manufacturing process or the raw material. This work studies the influence of quench and tempering and hot-dip galvanizing on the hydrogen embrittlement behavior of a high strength steel. Slow strain rate tensile testing has been employed to assess this influence. Two sets of specimens have been tested both in air and immersed in synthetic seawater at three process steps: in the delivery condition of the raw material after heat treatment and after heat treatment plus hot-dip galvanizing. One of the specimen sets has been tested without further manipulation and the other set has been tested after applying a hydrogen effusion treatment. The outcome for this case study is that fracture risk issues only arise due to hydrogen re-embrittlement in wet service.

Hydrogen technologies have been rapidly developing in the past few decades pushed by governments’ road maps for sustainability and supported by a widespread need to decarbonize the global energy sector. Recent scientific progress has led to better performances and higher efficiencies of hydrogen-related technologies so much so that their future economic viability is now rarely called into question. This article intends to study the integration of hydrogen systems in both gas and electric distribution networks. A preliminary analysis of hydrogen’s physical storage methods is given considering both the advantages and disadvantages of each one. After examining the preeminent ways of physically storing hydrogen this paper then contemplates two primary means of using it: integrating it in Power-to-Gas networks and utilizing it in Power-to-Power smart grids. In the former the primary objective is the total replacement of natural gas with hydrogen through progressive blending procedures from the transmission pipeline to the domestic burner; in the latter the set goal is the expansion of the implementation of hydrogen systems—namely storage—in multi-microgrid networks thus helping to decarbonize the electricity sector and reducing the impact of renewable energy’s intermittence through Demand Side Management strategies. The study concludes that hydrogen is assumed to be an energy vector that is inextricable from the necessary transition to a cleaner more efficient and sustainable future.

The present work provides an overview of the work on the interaction between hydrogen (H) and the steel’s microstructure. Different techniques are used to evaluate the H-induced damage phenomena. The impact of H charging on multiphase high-strength steels i.e. high-strength low-alloy (HSLA) transformation-induced plasticity (TRIP) and dual phase (DP) is first studied. The highest hydrogen embrittlement resistance is obtained for HSLA steel due to the presence of Ti- and Nb-based precipitates. Generic Fe-C lab-cast alloys consisting of a single phase i.e. ferrite bainite pearlite or martensite and with carbon contents of approximately 0 0.2 and 0.4 wt % are further considered to simplify the microstructure. Finally the addition of carbides is investigated in lab-cast Fe-C-X alloys by adding a ternary carbide forming element to the Fe-C alloys. To understand the H/material interaction a comparison of the available H trapping sites the H pick-up level and the H diffusivity with the H-induced mechanical degradation or H-induced cracking is correlated with a thorough microstructural analysis.

The development of a hydrogen-based economy is the perfect nexus between the need of discontinuing the use of fossil fuels (trying to mitigate climate change) the development of a system based on renewable energy (with the use of hydrogen allowing us to buffer the discontinuities produced in this generation) and the achievement of a local-based robust energy supply system. However extending the use of hydrogen as an energy vector must still overcome challenging issues with the key issues being related to its storage. Cryogenic or pressurized storage is relatively expensive technically complex and presents important safety concerns. As a promising alternative the use of organic hydrogen carriers has been suggested in recent years. The ideal carrier will be an organic compound with a low melting point and low viscosity with a significant number of unsaturated carbon–carbon bonds in addition to being easy to hydrogenate and dehydrogenate. These properties allow us to store and transport hydrogen in infrastructures designed for liquid fuels thus facilitating the replacement of fossil fuels by hydrogen

This study investigated the influence of segregations on hydrogen environment embrittlement (HEE) of AISI 304L type austenitic stainless steels. The microstructure of tensile specimens that were fabricated from commercially available AISI 304L steels and tested by means of small strain-rate tensile tests in air as well as hydrogen gas at room temperature was investigated by means of combined EDS and EBSD measurements. It was shown that two different austenitic stainless steels having the same nominal alloy composition can exhibit different susceptibilities to HEE due to segregation effects resulting from different production routes (continuous casting/electroslag remelting). Local segregation-related variations of the austenite stability were evaluated by thermodynamic and empirical calculations. The alloying element Ni exhibits pronounced segregation bands parallel to the rolling direction of the material which strongly influences the local austenite stability. The latter was revealed by generating and evaluating two-dimensional distribution maps for the austenite stability. The formation of deformation-induced martensite was shown to be restricted to segregation bands with a low Ni content. Furthermore it was shown that the formation of hydrogen induced surface cracks is strongly coupled with the existence of surface regions of low Ni content and accordingly low austenite stability. In addition the growth behavior of hydrogen-induced cracks was linked to the segregation-related local austenite stability.