Transmission, Distribution & Storage

Detailed heat exchanger designs are determined by matching intermediate temperatures in a large-scale Claude refrigeration process for liquefaction of hydrogen with a capacity of 125 tons/day. A comparison is made of catalyst filled plate-fin and spiral-wound heat exchangers by use of a flexible and robust modelling framework for multi-stream heat exchangers that incorporates conversion of ortho-to para-hydrogen in the hydrogen feed stream accurate thermophysical models and a distributed resolution of all streams and wall temperatures. Maps of the local exergy destruction in the heat exchangers are presented which enable the identification of several avenues to improve their performances.<br/>The heat exchanger duties vary between 1 and 31 MW and their second law energy efficiencies vary between 72.3% and 96.6%. Due to geometrical constraints imposed by the heat exchanger manufacturers it is necessary to employ between one to four parallel plate-fin heat exchanger modules while it is possible to use single modules in series for the spiral-wound heat exchangers. Due to the lower surface density and heat transfer coefficients in the spiral-wound heat exchangers their weights are 2–14 times higher than those of the plate-fin heat exchangers.<br/>In the first heat exchanger hydrogen feed gas is cooled from ambient temperature to about 120 K by use of a single mixed refrigerant cycle. Here most of the exergy destruction occurs when the high-pressure mixed refrigerant enters the single-phase regime. A dual mixed refrigerant or a cascade process holds the potential to remove a large part of this exergy destruction and improve the efficiency. In many of the heat exchangers uneven local exergy destruction reveals a potential for further optimization of geometrical parameters in combination with process parameters and constraints.<br/>The framework presented makes it possible to compare different sources of exergy destruction on equal terms and enables a qualified specification on the maximum allowed pressure drops in the streams. The mole fraction of para-hydrogen is significantly closer to the equilibrium composition through the entire process for the spiral-wound heat exchangers due to the longer residence time. This reduces the exergy destruction from the conversion of ortho-hydrogen and results in a higher outlet mole fraction of para-hydrogen from the process.<br/>Because of the higher surface densities of the plate-fin heat exchangers they are the preferred technology for hydrogen liquefaction unless a higher conversion to heat exchange ratio is desired.

Transition metal carbides are a class of materials widely known for both their interesting physical properties and catalytic activity. In this work we have used plane-wave DFT methods to study the interaction with increasing amounts of molecular hydrogen on the low-index surfaces of four major carbides – TiC VC ZrC and NbC. Adsorption is found to be generally exothermic and occurs predominantly on the surface carbon atoms. We identify trends over the carbides and their surfaces for the energetics of the adsorption as a function of their electronic and geometrical characteristics. An ab initio thermodynamics formalism is used to study the properties of the slabs as the hydrogen coverage is increased.

Carbon capture and storage (CCS) technologies are expected to play a significant part in the global climate response. Following the ratification of the Paris Agreement the ability of CCS to reduce emissions from fossil fuel use in power generation and industrial processes – including from existing facilities – will be crucial to limiting future temperature increases to ""well below 2°C"" as laid out in the Agreement. CCS technology will also be needed to deliver ""negative emissions"" in the second half of the century if these ambitious goals are to be achieved.

CCS technologies are not new. This year is the 20th year of operation of the Sleipner CCS Project in Norway which has captured almost 17 million tonnes of CO2 from an offshore natural gas production facility and permanently stored them in a sandstone formation deep under the seabed. Individual applications of CCS have been used in industrial processes for decades and projects injecting CO2 for enhanced oil recovery (EOR) have been operating in the United States since the early 1970s.

This publication reviews progress with CCS technologies over the past 20 years and examines their role in achieving 2°C and well below 2°C targets. Based on the International Energy Agency’s 2°C scenario it also considers the implications for climate change if CCS was not a part of the response. And it examines opportunities to accelerate future deployment of CCS to meet the climate goals set in the Paris Agreement.

Link to Document on IEA Website

High susceptibility to cold cracking induced by diffusible hydrogen and hydrogen embrittlement are major obstacles to greater utilization of underwater wet welding for high-strength steels. The aim of the research was to develop gas–slag systems for flux-cored wires that have high metallurgical activity in removal of hydrogen and hydroxyl groups. Thermodynamic modeling and experimental research confirmed that a decrease in the concentration of diffusible hydrogen can be achieved by reducing the partial pressure of hydrogen and water vapor in the vapor–gas bubble and by increasing the hydroxyl capacity of the slag system in metallurgical reactions leading to hydrogen fluoride formation and ionic dissolution of hydroxyl groups in the basic fluorine-containing slag of a TiO2–CaF₂–Na₃AlF₆ system.

The influence of the addition of refractory metals (molybdenum and tantalum) on the hydrogenation properties of FeTi intermetallic phase-based alloys was investigated. The suspended droplet alloying technique was applied to fabricate FeTiTa-based and FeTiMo-based alloys. The phase composition and hydrogen storage properties of the samples were investigated. The samples modified with the refractory metals exhibited lower plateau pressures and lower hydrogen storage capacities than those of the FeTi reference sample due to solid solution formation. It was observed that the equilibrium pressures decreased with the amount of molybdenum which is in good agreement with the increase in the cell parameters of the TiFe phase. Suspended droplet alloying was found to be a practical method to fabricate alloys with refractory metal additions; however it is appropriate for screening samples with desired chemical and phase compositions rather than for manufacturing purposes.

This paper reports a new approach for exposing materials including solar cell structures to atomic hydrogen. This method is dubbed Shielded Hydrogen Passivation (SHP) and has a number of unique features offering high levels of atomic hydrogen at low temperature whilst inducing no damage. SHP uses a thin metallic layer in this work palladium between a hydrogen generating plasma and the sample which shields the silicon sample from damaging UV and energetic ions while releasing low energy neutral atomic hydrogen onto the sample. In this paper the importance of the preparation of the metallic shield either to remove a native oxide or to contaminate intentionally the surface are shown to be potential methods for increasing the amount of atomic hydrogen released. Excellent damage free surface passivation of thin oxides is observed by combining SHP and corona discharge obtaining minority carrier lifetimes of 2.2 ms and J0 values below 5.47 fA/cm2. This opens up a number of exciting opportunities for the passivation of advanced cell architectures such as passivated contacts and heterojunctions.

DFT calculations at B3LYP/6-31g(dp) with the D3 version of Grimme’s dispersion are performed to investigate the application of TM-encapsulated Mg12O12 nano-cages (TM= Mn Fe and Co) as a hydrogen storage material. The molecular dynamic (MD) calculations are utilized to examine the stability of the considered structures. TD-DFT method reveals that the TM-encapsulation converts the Mg12O12 from an ultraviolet into a visible optical active material. The adsorption energy values indicate that the Mn and Fe atoms encapsulation enhances the adsorption of H2 molecules on the Mg12O12 nano-cage. The pristine Mg12O12 and CoMg12O12 do not meet the requirements for hydrogen storage materials while the MnMg12O12 and FeMg12O12 obey the requirements. MnMg12O12 and FeMg12O12 can carry up to twelve and nine H2 molecules respectively. The hydrogen adsorption causes a redshift for the λmax value of the UV-Vis. spectra of the MnMg12O12 and FeMg12O12 nano-cages. The thermodynamic calculations show that the hydrogen storage reaction for MnMg12O12 nano-cage is a spontaneous reaction while for FeMg12O12 nano-cage is not spontaneous. The results suggested that the MnMg12O12 nano-cage may be a promising material for hydrogen storage applications.

Hydrogen transport and trapping equations are implemented in a FE software using User Subroutines and the obtained tool is applied to get the diffusion fields in a metallic sheet submitted to a U-Bend test. Based on a submodelling process mechanical and diffusion fields have been computed at the polycrystal scale from which statistical evaluation of the risk of failure of the sample has been estimated.

The objective of this work is to investigate the effect of hydrogen-induced fracture of TiNi-based alloy. In this report we performed the first studies comparing inelastic properties and fracture of the specimens of the binary alloy of TiNi wire under the action of hydrogen with coarse-grained (CG) and ultrafine-grained (UFG) microstructure. It is shown that hydrogen embrittlement (HE) occurs irrespective of the grain size in the studied specimens at approximately equal strain values. However compared to the specimens with CG structure those with UFG structure accumulate two to three times more hydrogen for the same hydrogenation time. It is found that hydrogen has a much smaller effect on the inelastic properties of specimens with UFG structure as compared to those with CG structure.

Effects of hydrogen on slow-strain-rate tensile (SSRT) and fatigue-life properties of 17-4PH H1150 martensitic stainless steel having an ultimate tensile strength of ~1GPa were investigated. Smooth and circumferentially-notched axisymmetric specimens were used for the SSRT and fatigue-life tests respectively. The fatigue-life tests were done to investigate the hydrogen effect on fatigue crack growth (FCG) properties. The specimens tested in air at ambient temperature were precharged by exposure to hydrogen gas at pressures of 35 and 100 MPa at 270°C for 200 h. The SSRT properties of the H-charged specimens were degraded by hydrogen showing a relative reduction in area (RRA) of 0.31 accompanied by mixed fracture surfaces composed of quasi-cleavage (QC) and intergranular cracking (IG). The fatigue-life tests conducted under wide test frequencies ranging from 10-3 Hz to 10 Hz revealed three distinct characteristics in low- and high-cycle regimes and at the fatigue limit. The fatigue limit was not degraded by hydrogen. In the high-cycle regime the hydrogen caused FCG acceleration with an upper bound ratio of 30 accompanied by QC surfaces. In the low-cycle regime the hydrogen caused FCG acceleration with a ratio of ~100 accompanied by QC and IG. The ordinary models such as process competition and superposition models hardly predicted the H-assisted FCG acceleration; therefore an interaction model successfully reproducing the experimental FCG acceleration was newly introduced.

In 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 min in a 100 L 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.

Some illustrations of the use of deuterium or tritium for isotopic tracing of hydrogen absorption transport and trapping in nuclear materials are presented. Isotopic tracing of hydrogen has been shown to be successful for the determination of the boundaries conditions for hydrogen desorption or absorption in a material exposed to a hydrogen source. Also the unique capabilities of isotopic tracing and related techniques to characterize H interactions with point defects and dislocations acting as moving traps has been demonstrated. Such transport mechanisms are considered to play a major role in some stress corrosion cracking and hydrogen embrittlement mechanisms.

Link to document download on Royal Society Website  

In this study YMg₁₁Ni and YMg₁₁Ni + 5 wt% MoS₂ (named YMg11Ni–MoS₂) alloys were prepared by mechanical milling to examine the effect of adding MoS₂ on the hydrogen storage performance of a Y–Mg–Ni-based alloy. The as-cast and milled alloys were tested to identify their structures by X-ray diffraction and transmission electron microscopy. The isothermal hydrogen storage thermodynamics and dynamics were identified through an automatic Sieverts apparatus and the non-isothermal dehydrogenation performance was investigated by thermogravimetry and differential scanning calorimetry. The dehydrogenation activation energy was calculated by both Arrhenius and Kissinger methods. Results revealed that adding MoS₂produces a very slight effect on hydrogen storage thermodynamics but causes an obvious reduction in the hydrogen sorption and desorption capacities because of the deadweight of MoS_2. The addition of MoS₂significantly enhances the dehydrogenation performance of the alloy such as lowering dehydrogenation temperature and enhancing dehydrogenation rate. Specifically the initial desorption temperature of the alloy hydride lowers from 549.8 K to 525.8 K. The time required to desorb hydrogen at 3 wt% H₂ is 1106 456 363 and 180 s corresponding to hydrogen desorption temperatures at 593 613 633 and 653 K for the YMg₁₁Ni alloy and 507 208 125 and 86 s at identical conditions for the YMg₁₁Ni–5MoS₂ alloy. The dehydrogenation activation energy (E_a) values with and without added MoS₂are 85.32 and 98.01 kJ mol⁻¹. Thus a decrease in E_a value by 12.69 kJ mol−1 occurs and is responsible for the amelioration of the hydrogen desorption dynamics by adding a MoS₂ catalyst.

Efficient energy production and consumption are fundamental points for reducing carbon emissions that influence climate change. Alternative resources such as renewable energy sources (RESs) used in electricity grids could reduce the environmental impact. Since RESs are inherently unreliable during the last decades the scientific community addressed research efforts to their integration with the main grid by means of properly designed energy storage systems (ESSs). In order to highlight the best performance from these hybrid systems proper design and operations are essential. The purpose of this paper is to present a so-called model predictive controller (MPC) for the optimal operations of grid-connected wind farms with hydrogen-based ESSs and local loads. Such MPC has been designed to take into account the operating and economical costs of the ESS the local load demand and the participation to the electricity market and further it enforces the fulfillment of the physical and the system's dynamics constraints. The dynamics of the hydrogen-based ESS have been modeled by means of the mixed-logic dynamic (MLD) framework in order to capture different behaviors according to the possible operating modes. The purpose is to provide a controller able to cope both with all the main physical and operating constraints of a hydrogen-based storage system including the switching among different modes such as ON OFF STAND-BY and at the same time reduce the management costs and increase the equipment lifesaving. The case study for this paper is a plant under development in the north Norway. Numerical analysis on the related plant data shows the effectiveness of the proposed strategy which manages the plant and commits the equipment so as to preserve the given constraints and save them from unnecessary commutation cycles.

Strain-induced martensite transformation (SIMT) commonly exists around a crack tip of metastable austenite stainless steels. The influence of the volume expansion of the SIMT on the hydrogen diffusion was investigated by hydrogen diffusion modelling around a crack tip in type 304L austenite stainless steel. The volume expansion changed the tensile stress state into pressure stress state at the crack tip resulting in a large stress gradient along the crack propagation direction. Compared to the analysis without considering the volume expansion effect this volume expansion further accelerated the hydrogen transport from the inner surface to a critical region ahead of the crack tip and further increased the maximum value of the hydrogen concentration at the critical position where the strain-induced martensite fraction approximates to 0.1 indicating that the volume expansion of the SIMT further increased the hydrogen embrittlement susceptibility.

Grand Canonical Monte Carlo GCMC simulations are used to study the gravimetric and volumetric hydrogen storage capacities of different carbon nanopores shapes: Slit-shaped nanotubes and torusenes at room temperature 298.15 K and at pressures between 0.1 and 35 MPa and for pore diameter or width between 4 and 15 A. The influence of the pore shape or curvature on the storage capacities as a function of pressure temperature and pore diameter is investigated and analyzed. A large curvature of the pores means in general an increase of the storage capacities of the pores. While torusenes and nanotubes have surfaces with more curvature than the slit-shaped planar pores their capacities are lower than those of the slit-shaped pores according to the present GCMC simulations. Torusene a less studied carbon nanostructure has two radii or curvatures but their storage capacities are similar or lower than those of nanotubes which have only one radius or curvature. The goal is to obtain qualitative and quantitative relationships between the structure of porous materials and the hydrogen storage capacities in particular or especially the relationship between shape and width of the pores and the hydrogen storage capacities of carbon-based porous materials.

Development of probabilistic modelling tools to perform Bayesian inference and uncertainty quantification (UQ) is a challenging task for practical hydrogen-enriched and low-emission combustion systems due to the need to take into account simultaneously simulated fluid dynamics and detailed combustion chemistry. A large number of evaluations is required to calibrate models and estimate parameters using experimental data within the framework of Bayesian inference. This task is computationally prohibitive in high-fidelity and deterministic approaches such as large eddy simulation (LES) to design and optimize combustion systems. Therefore there is a need to develop methods that: (a) are suitable for Bayesian inference studies and (b) characterize a range of solutions based on the uncertainty of modelling parameters and input conditions. This paper aims to develop a computationally-efficient toolchain to address these issues for probabilistic modelling of NOx emission in hydrogen-enriched and lean-premixed combustion systems. A novel method is implemented into the toolchain using a chemical reactor network (CRN) model non-intrusive polynomial chaos expansion based on the point collocation method (NIPCE-PCM) and the Markov Chain Monte Carlo (MCMC) method. First a CRN model is generated for a combustion system burning hydrogen-enriched methane/air mixtures at high-pressure lean-premixed conditions to compute NOx emission. A set of metamodels is then developed using NIPCE-PCM as a computationally efficient alternative to the physics-based CRN model. These surrogate models and experimental data are then implemented in the MCMC method to perform a two-step Bayesian calibration to maximize the agreement between model predictions and measurements. The average standard deviations for the prediction of exit temperature and NOx emission are reduced by almost 90% using this method. The calibrated model then used with confidence for global sensitivity and reliability analysis studies which show that the volume of the main-flame zone is the most important parameter for NOx emission. The results show satisfactory performance for the developed toolchain to perform Bayesian inference and UQ studies enabling a robust and consistent process for designing and optimising low-emission combustion systems.

Since the addition of Al to high-Mn steels is known to reduce their sensitivity to hydrogen-induced delayed fracture we investigate possible trapping effects connected to the presence of Al in the grain interior employing density-functional theory (DFT). The role of Al-based precipitates is also investigated to understand the relevance of short-range ordering effects. So-called E21-Fe3AlC κ-carbides are frequently observed in Fe-Mn-Al-C alloys. Since H tends to occupy the same positions as C in these precipitates the interaction and competition between both interstitials is also investigated via DFT-based simulations. While the individual H–H/C–H chemical interactions are generally repulsive the tendency of interstitials to increase the lattice parameter can yield a net increase of the trapping capability. An increased Mn content is shown to enhance H trapping due to attractive short-range interactions. Favorable short-range ordering is expected to occur at the interface between an Fe matrix and the E21-Fe3AlC κ-carbides which is identified as a particularly attractive trapping site for H. At the same time accumulation of H at sites of this type is observed to yield decohesion of this interface thereby promoting fracture formation. The interplay of these effects evident in the trapping energies at various locations and dependent on the H concentration can be expressed mathematically resulting in a term that describes the hydrogen embrittlement

The effects of hot stamping (HS) and tempering on the hydrogen embrittlement (HE) behavior of a low-carbon boron-alloyed steel were studied by using slow strain rate tensile (SSRT) tests on notched sheet specimens. It was found that an additional significant hydrogen desorption peak at round 65–80 °C appeared after hydrogen-charging the corresponding hydrogen concentration (CHr) of the HS specimen was higher than that of the directed quenched (DQ) specimen and subsequent low-temperature tempering gave rise to a decrease of CHr. The DQ specimen exhibited a comparatively high HE susceptibility while tempering treatment at 100 °C could notably alleviate it by a relative decrease of ~24% at no expanse of strength and ductility. The HS specimen demonstrated much lower HE susceptibility compared with the DQ specimen and tempering at 200 °C could further alleviate its HE susceptibility. SEM analysis of fractured SSRT surfaces revealed that the DQ specimen showed a mixed transgranular-intergranular fracture while the HS and low-temperature tempered specimens exhibited a predominant quasi-cleavage transgranular fracture. Based on the obtained results we propose that a modified HS process coupled with low-temperature tempering treatment is a promising and feasible approach to ensure a low HE susceptibility for high-strength automobile parts made of this type of steel.

Hydrogen has been long known to provide a solution toward clean energy systems. With this notion many efforts have been made to find new ways of storing hydrogen. As a result decades of studies has led to a wide range of hydrides that can store hydrogen in a solid form. Applications of these solid-state hydrides are well-suited to stationary applications. However the main challenge arises in making the selection of the Metal Hydrides (MH) that are best suited to meet application requirements. Herein we discuss the current state-of-art in controlling the properties of room temperature (RT) hydrides suitable for stationary application and their long term behavior in addition to initial activation their limitations and emerging trends to design better storage materials. The hydrogen storage properties and synthesis methods to alter the properties of these MH are discussed including the emerging approach of high-entropy alloys. In addition the integration of intermetallic hydrides in vessels their operation with fuel cells and their use as thermal storage is reviewed.

Hydrogen embrittlement susceptibility ratios calculated from slow strain rate tensile tests have been employed to study the response of three high-strength mooring steels in cold and warm synthetic seawater. The selected nominal testing temperatures have been 3 °C and 23 °C in order to resemble sea sites of offshore platform installation interest such as the North Sea and the Gulf of Mexico respectively. Three scenarios have been studied for each temperature: free corrosion cathodic protection and overprotection. An improvement on the hydrogen embrittlement tendency of the steels has been observed when working in cold conditions. This provides a new insight on the relevance of the seawater temperature as a characteristic to be taken into account for mooring line design in terms of hydrogen embrittlement assessment.

This paper presents a simplified procedure to analyse the Hydrogen Induced Cracking (HIC) of structural steels by means of the Small Punch Test (SPT). Two types of notched specimens were used: one with through-thickness lateral notch and another with surface longitudinal notch. The results for conventional specimens were compared with those for hydrogen pre-charged specimens. For this purpose two different methods to introduce hydrogen in the specimens were used: cathodic/electrochemical pre-charging and pressurized gaseous hydrogen pre-charging. The results obtained with both methods are also discussed.

Fracture failure caused by hydrogen embrittlement (HE) is a major concern for the system reliability and safety of hydrogen storage vessels which are generally made of 2.25Cr1Mo0.25V steel. Thus study of the influence of pre-charged hydrogen on fracture toughness of as-received 2.25Cr1Mo0.25V steel and weld is of significant importance. In the current work the influence of hydrogen on fracture toughness of as-received 2.25Cr1Mo0.25V steel and weld was systematically studied. Base metal (BM) and weld metal (WM) specimens under both hydrogen-free and hydrogen-charged conditions were tested using three-point bending tests. Hydrogen was pre-charged inside specimens by the immersion charging method. The J-integral values were calculated for quantitatively evaluating the fracture toughness. In order to investigate the HE mechanisms optical microscopy (OM) and scanning electron microscopy (SEM) were used to characterize the microstructure of BM and WM specimens. The results revealed that the presence of pre-charged hydrogen caused a significant decrease of the fracture toughness for both BM and WM specimens. Moreover the pre-charged hydrogen led to a remarkable transition of fracture mode from ductile to brittle pattern in 2.25Cr1Mo0.25V steel.

Underground storage is a method of storing large amounts of renewable energy that can be converted into hydrogen. One of the fundamental problems associated with this process concerns determining the timing and amount of injected gas in the first filling period for the operation of an underground storage facility. Ascertaining the hydrogen flow rate is essential to ensure that the capillary and fracturing pressures are not exceeded. The value of the flow rate was assessed by modelling the injection of hydrogen into a deep aquifer. The best initial H2 injection period was found to be five months. The volume of the cushion gas and the total storage capacity expanded with the extension of the first filling period length. The working capacity grew as the depth increased reaching maximum values at depths of approximately 1200e1400 m. This depth was considered optimal for storing hydrogen in the analysed structure.

In this podcast David Ledesma talks with Rahmat Poudineh and Martin Palovic about their paper on integrating hydrogen into the European energy transfer infrastructure landscape. As hydrogen is expected to play an important role in European plans towards climate neutrality adequate hydrogen transport (and storage) infrastructure needs to be established. However hydrogen transport infrastructures are costly and have a long lead time. Furthermore hydrogen can be transported via a variety of means: it can be transported as a gas via pipelines or liquid via road rail and sea or even converted to derivatives such as ammonia or methanol for long distance transportation. It is also possible to transfer electrical energy instead of hydrogen and produce hydrogen in a decentralized way. From a system perspective all these infrastructures represent elements of a grand hydrogen ‘polygrid’ that will be the backbone of the future decarbonized energy system. This raises the fundamental question of how to prevent inefficiency and infrastructure redundancy across different modes of hydrogen transport. The task is made more challenging by technological uncertainty the unpredictability of future supply and demand for hydrogen network externality effects and investment irreversibility of grid-based infrastructures. In this podcast we discuss three possible coordination approaches to optimise future cross-sectoral investment into hydrogen transport infrastructure and highlight their strengths and shortcomings.

The podcast can be found on their website.