Japan

The location of hydrogen within Ti–Cr–V–Mo alloys has been investigated during hydrogen absorption and desorption using in situ neutron powder diffraction and inelastic neutron scattering. Neutron powder diffraction identifies a low hydrogen equilibration pressure body-centred tetragonal phase that undergoes a martensitic phase transition to a face-centred cubic phase at high hydrogen equilibration pressures. The average location of the hydrogen in each phase has been identified from the neutron powder diffraction data although inelastic neutron scattering combined with density functional theory calculations show that the local structure is more complex than it appears from the average structure. Furthermore the origin of the change in dissociation pressure and hydrogen trapping on cycling in Ti–Cr–V–Mo alloys is discussed.

‟How crack growth is prevented” is key to improve both fatigue and monotonic fracture resistances under an influence of hydrogen. Specifically the key points for the crack growth resistance are hydrogen diffusivity and local ductility. For instance type 304 austenitic steels show high hydrogen embrittlement susceptibility because of the high hydrogen diffusivity of bcc (α´) martensite. In contrast metastability in specific austenitic steels enables fcc (γ) to hcp (ε) martensitic transformation which decreases hydrogen diffusivity and increases strength simultaneously. As a result even if hydrogen-assisted cracking occurs during monotonic tensile deformation the ε-martensite acts to arrest micro-damage evolution when the amount of ε-martensite is limited. Thus the formation of ε-martensite can decrease hydrogen embrittlement susceptibility in austenitic steels. However a considerable amount of ε-martensite is required when we attempt to have drastic improvements of work hardening capability and strength level with respect to transformation-induced plasticity effect. Since the hcp structure contains a less number of slip systems than fcc and bcc the less stress accommodation capacity often causes brittle-like failure when the ε-martensite fraction is large. Therefore ductility of ε-martensite is another key when we maximize the positive effect of ε-martensitic transformation. In fact ε-martensite in a high entropy alloy was recently found to be extraordinary ductile. Consequently the metastable high entropy alloys showed low fatigue crack growth rates in a hydrogen atmosphere compared with conventional metastable austenitic steels with α´-martensitic transformation. We here present effects of metastability to ε-phase and configurational entropy on hydrogen-induced mechanical degradation including monotonic tension properties and fatigue crack growth resistance.

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.

Hydrogen and its energy carriers such as liquid hydrogen (LH2) methylcyclohexane (MCH) and ammonia (NH3) are essential components of low-carbon energy systems. To utilize hydrogen energy the complete environmental merits of its supply chain should be evaluated. To understand the expected environmental benefit under the uncertainty of hydrogen technology development we conducted life-cycle inventory analysis and calculated CO2 emissions and their uncertainties attributed to the entire supply chain of hydrogen and NH3 power generation (co-firing and mono-firing) in Japan. Hydrogen was assumed to be produced from overseas renewable energy sources with LH2/MCH as the carrier and NH3 from natural gas or renewable energy sources. The Japanese life-cycle inventory database was used to calculate emissions. Monte Carlo simulations were performed to evaluate emission uncertainty and mitigation factors using hydrogen energy. For LH2 CO2 emission uncertainty during hydrogen liquefaction can be reduced by using low-carbon fuel. For MCH CO2 emissions were not significantly affected by power consumption of overseas processes; however it can be reduced by implementing low-carbon fuel and waste-heat utilization during MCH dehydrogenation. Low-carbon NH3 production processes significantly affected power generation whereas carbon capture and storage during NH3 production showed the greatest reduction in CO2 emission. In conclusion reducing CO2 emissions during the production of hydrogen and NH3 is key to realize low-carbon hydrogen energy systems.

The aim of this study is to provide a quantification of the internal pressure contribution to the SSRT properties of H-charged Type-316L steel tested in air at room temperature. Considering pre-existing penny-shaped voids the transient pressure build-up has been simulated as well as its impact on the void growth by preforming JIc calculations. Several void distributions (size and spacing) have been considered. Simulations have concluded that there was no impact of the internal pressure on the void growth regardless the void distribution since the effective pressure was on the order of 1 MPa during the SSRT test. Even if fast hydrogen diffusion related to dislocation pipe-diffusion has been assessed as a conservative case the impact on void growth was barely imperceptible (or significantly low). The effect of internal pressure has been experimentally verified via the following conditions: (I) non-charged in vacuum; (II) H-charged in vacuum; (III) H-charged in 115-MPa nitrogen gas; (IV) non-charged in 115-MPa nitrogen gas. As a result the relative reduction in area (RRA) was 0.84 for (II) 0.88 for (III) and 1.01 for (IV) respectively. The difference in void morphology of the H-charged specimens did not depend on the presence of external pressure. These experimental results demonstrate that the internal pressure had no effect on the tensile ductility and void morphology of the H-charged specimen.

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.

In this study the combustion of submicron-sized Al particles in air was studied numerically with a particular focus on the effect of hydrogen addition. Oxidation of the Al particles and the interaction with hydrogen-related intermediates were considered by regarding them as liquid-phase molecules initially. Zero- and One-dimensional numerical simulations were then carried out to investigate the effect of the hydrogen addition on fundamental combustion characteristics of the Al flame by calculating properties such as ignition delay time and flame speed. Our attention was paid to how the hydrogen chemistry is coupled with the Al oxidation process. Numerical results show that the hydrogen addition generally reduces the reactivity of Al such that the flame speed and temperature decrease while it  can greatly shorten ignition delay times of the Al flame depending on initial temperatures.

The effects of different mole fractions of hydrogen and carbon dioxide on the combustion characteristics of a premixed methane–air mixture are experimentally and numerically investigated. The laminar burning velocity of hydrogen-methane-carbon dioxide-air mixture was measured using the spherically expanding flame method at the initial temperature and pressure of 283 K and 0.1 MPa respectively. Additionally numerical analysis is conducted under steady 1D laminar flow conditions to investigate the adiabatic flame temperature and dominant elementary reactions. The measured velocities correspond with those estimated numerically. The results show that increasing the carbon dioxide mole fraction decreases the laminar burning velocity attributed to the carbon dioxide dilution which decreases the thermal diffusivity and flame temperature. Conversely the velocity increases with the thermal diffusivity as the hydrogen mole fraction increases. Moreover the hydrogen addition leads to chain-branching reactions that produce active H O and OH radicals via the oxidation of hydrocarbons which is the rate-determining reaction.

Hydrogen energy utilization is expected due to its environmental and energy efficiencies. However many issues remain to be solved in the social implementation of hydrogen energy through water electrolysis. This analyzes and compares the energy consumption and GHG emissions of fossil fuel-derived hydrogen and gasoline energy systems over their entire life cycle. The results demonstrate that for similar vehicle weights the hydrogen energy system consumes 1.8 MJ/km less energy and emits 0.15 kg-CO 2 eq./km fewer GHG emissions than those of the gasoline energy system. Hydrogen derived from fossil fuels may contribute to future energy systems due to its stable energy supply and economic efficiency. Lowering the power source carbon content also improved the environmental and energy efficiencies of hydrogen energy derived from fossil fuels.

This study reviews the extant literature on hydrogen production cost forecasts to identify and analyze the historical trend of such forecasts in order to explore the feasibility of wider adoption. Hydrogen is an important energy source that can be used to achieve a carbon-neutral society but the widespread adoption of hydrogen production technologies is hampered by the high costs. The production costs vary depending on the technology employed: gray renewable electrolysis or biomass. The study identifies 174 production cost forecast data points from articles published between 1979 and 2020 and makes a comparative assessment using non-parametric statistical tests. The results show three different cost forecast trends across technologies. First the production cost of gray hydrogen showed an increasing trend until 2015 but started declining after 2015. Second the renewable electrolysis hydrogen cost was the highest of all but has shown a gradual declining trend since 2015. Finally the biomass hydrogen cost has been relatively cheaper up until 2015 after which it became the highest. Renewable electrolysis and biomass hydrogen will be potential candidates (as principal drivers) to reduce CO2 emissions in the future but renewable electrolysis hydrogen is more promising in this regard due to its declining production cost trend. Gray hydrogen can also be an alternative candidate to renewable electrolysis hydrogen because it can be equipped with carbon capture storage (CCS) to produce blue hydrogen although we need to consider additional production costs incurred by the introduction of CCS. The study discusses the technological development and policy implications of the results on hydrogen production costs.