Transmission, Distribution & Storage

A polyethylene (PE) liner is the basic element in high-pressure type 4 composite vessels designed for hydrogen or compressed natural gas (CNG) storage systems. Liner defects may result in the elimination of the whole vessel from use which is very expensive both at the manufacturing and exploitation stage. The goal is therefore the development of efficient non-destructive testing (NDT) methods to test a liner immediately after its manufacturing before applying a composite reinforcement. It should be noted that the current regulations codes and standards (RC&S) do not specify liner testing methods after manufacturing. It was considered especially important to find a way of locating and assessing the size of air bubbles and inclusions and the field of deformations in liner walls. It was also expected that these methods would be easily applicable to mass-produced liners. The paper proposes the use of three optical methods namely visual inspection digital image correlation (DIC) and optical fiber sensing based on Bragg gratings (FBG). Deformation measurements are validated with finite element analysis (FEA). The tested object was a prototype of a hydrogen liner for high-pressure storage (700 bar). The mentioned optical methods were used to identify defects and measure deformations.

Three techniques for determining the hydrogen permeation properties of rubber samples were developed based on the volumetric and gravimetric measurements of released H2 gas after sample decompression. These methods include gas chromatography (GC) by thermal desorption analysis (TDA) volumetric collection (VC) measurement of hydrogen by graduated cylinder and gravimetric (GM) measurement by electronic balance. By measuring the released hydrogen against elapsed time after the decompression of pressure the charging amount (C0) and diffusivity (D) were obtained with the developed diffusion analysis program. From these values the solubility (S) and permeability (P) of polymers were evaluated through the relations of Henry's law and P=SD respectively. The developed techniques were applied to three kinds of spherically shaped sealing rubber materials. D S and P were analyzed as a function of pressure. The transport behaviors obtained in the three methods are discussed and compared with the characteristics of each measuring technique. The correlations between transport parameters and carbon black filler or density are discussed.

Stress corrosion cracking (SCC) of metals is an issue of major concern in engineering since this phenomenon causes many catastrophic failures of structural components in aggressive environments. SCC is even more harmful under cathodic conditions promoting the phenomenon known as hydrogen assisted cracking (HAC) hydrogen assisted fracture (HAF) or hydrogen embrittlement (HE). A common way to assess the susceptibility of a given material to HAC HAF or HE is to subject a cracked rod to a constant extension rate tension (CERT) test until it fractures in this harsh environment. This paper analyzes the influence of a residual stress field generated by fatigue precracking on the sample’s posterior susceptibility to HAC. To achieve this goal numerical simulations were carried out of hydrogen diffusion assisted by the stress field. Firstly a mechanical simulation of the fatigue precracking was developed for revealing the residual stress field after diverse cyclic loading scenarios and posterior stress field evolution during CERT loading. Afterwards a simulation of hydrogen diffusion assisted by stress was carried out considering the residual stresses after fatigue and the superposed rising stresses caused by CERT loading. Results reveal the key role of the residual stress field after fatigue precracking in the HAC phenomena in cracked steel rods as well as the beneficial effect of compressive residual stress.

This paper analyzes using the theory of critical distances the environmentally assisted cracking behaviour of two steels (S420 and API X80) subjected to two different aggressive environments. The propagation threshold for environmentally assisted cracking (i.e. the stress intensity factor above which crack propagation initiates) in cracked and notched specimens (KIEAC and KNIEAC) has been experimentally obtained under different environmental conditions. Cathodic polarization has been employed to generate the aggressive environments at 1 and 5 mA/cm² causing hydrogen embrittlement on the steels. The point method and the line method both belonging to the theory of critical distances have been applied to verify their capacity to predict the initiation of crack propagation. The results demonstrate the capacity of the theory of critical distances to predict the crack propagation onset under the different combinations of material and aggressive environments.

The growing of fossil fuel burning leads to increase CO2 and H2 emissions which cause increasing of global warming that has brought big attention. As a result enormous researches have been made to reduce CO2 and H2 build up in the environment. One of the most promising approaches for managing CO2 and H2 gases percentage in the atmosphere is capturing and storage them inside proper materials. Therefore the design of new materials for carbon dioxide and hydrogen storage has received increasing research attention. Four derivatives of coumarine linked to thiazolidinone were synthesized in good yields by reacting 3-(2-Phenylaminoacetyl)coumarine and 2-phenylimino thiazolidinone-4-one in a solution of anhydrous sodium acetate /glacial acetic acid at 120° for 5-6 hours. The synthesised organic compounds were identified by using different techniques such as 1H NMR 13C NMR FTIR and energy dispersive X-ray spectra. The agglomeration shape and porosity of the particles were determined utilizing scanning electron microscopy (SEM) and microscopy images analysis. The capacity of carbon dioxide (CO2) and hydrogen (H2) adsorption on the prepared organic materials at 323 K 50 bar ranged from 22 to 31 cm3 /g and hydrogen from 4 to 12 cm3 /g for the four synthesised compounds which contain phenyl substituted with chloro nitro and bromo groups was found to be the most active adsorbent surfaces for carbon dioxide and hydrogen storage.

Hydrogen is often described as the fuel of the future especially for application in hydrogen powered fuel-cell vehicles (HFCV’s). However its widespread implementation in this role has been thwarted by the lack of a lightweight safe on-board hydrogen storage material. Here we show that benign readily available hydrocarbon wax is capable of rapidly releasing large amounts of hydrogen through microwave-assisted catalytic decomposition. This discovery offers a new material and system for safe and efficient hydrogen storage and could facilitate its application in a HFCV. Importantly hydrogen storage materials made of wax can be manufactured through completely sustainable processes utilizing biomass or other renewable feedstocks.

TiFe activation for hydrogen uptake was conducted through different methods and ball milling with ethanol proved to be the most effective one. TiFe alloy after activation could absorb 1.2 wt% hydrogen at room temperature with absorption and desorption plateaus of 0.5 MPa and 0.2 MPa respectively. Investigation on microstructure and chemical state of TiFe sample after milled with ethanol suggested that the well spread metallic Ti and Fe elements helped hydrogen uptake and release. The activation of TiFe alloy by milling with ethanol was achieved at ambient conditions with ease successfully and possibly can be used for large scale production

A promising option for storing large-scale quantities of green gases (e.g. hydrogen) is in subsurface rock salt caverns. The mechanical performance of salt caverns utilized for long-term subsurface energy storage plays a signifcant role in long-term stability and serviceability. However rock salt undergoes non-linear creep deformation due to long-term loading caused by subsurface storage. Salt caverns have complex geometries and the geological domain surrounding salt caverns has a vast amount of material heterogeneity. To safely store gases in caverns a thorough analysis of the geological domain becomes crucial. To date few studies have attempted to analyze the infuence of geometrical and material heterogeneity on the state of stress in salt caverns subjected to long-term loading. In this work we present a rigorous and systematic modeling study to quantify the impact of heterogeneity on the deformation of salt caverns and quantify the state of stress around the caverns. A 2D fnite element simulator was developed to consistently account for the non-linear creep deformation and also to model tertiary creep. The computational scheme was benchmarked with the already existing experimental study. The impact of cyclic loading on the cavern was studied considering maximum and minimum pressure that depends on lithostatic pressure. The infuence of geometric heterogeneity such as irregularly-shaped caverns and material heterogeneity which involves diferent elastic and creep properties of the diferent materials in the geological domain is rigorously studied and quantifed. Moreover multi-cavern simulations are conducted to investigate the infuence of a cavern on the adjacent caverns. An elaborate sensitivity analysis of parameters involved with creep and damage constitutive laws is performed to understand the infuence of creep and damage on deformation and stress evolution around the salt cavern confgurations.

Using hydrogen as an energy carrier requires new technological solutions for its onboard storage. The exploration of two-dimensional (2D) materials for hydrogen storage technologies has been motivated by their open structures which facilitates fast hydrogen kinetics. Herein the hydrogen storage properties of lightweight metal functionalized r57 haeckelite sheets are studied using density functional theory (DFT) calculations. H₂ molecules are adsorbed on pristine r₅₇ via physisorption. The hydrogen storage capacity of r₅₇ is improved by decorating it with alkali and alkaline-earth metals. In addition the in-plane substitution of r57 carbons with boron atoms (B@r57) both prevents the clustering of metals on the surface of 2D material and increases the hydrogen storage capacity by improving the adsorption thermodynamics of hydrogen molecules. Among the studied compounds B@r57-Li4 with its 10.0 wt% H₂ content and 0.16 eV/H₂ hydrogen binding energy is a promising candidate for hydrogen storage applications. A further investigation as based on the calculated electron localization functions atomic charges and electronic density of states confirm the electrostatic nature of interactions between the H₂ molecules and the protruding metal atoms on 2D haeckelite sheets. All in all this work contributes to a better understanding of pure carbon and B-doped haeckelites for hydrogen storage.

The composites comprised of Co nanoparticle and C nanosheet were prepared though a high-temperature carbonization reaction. The catalysis of Co@C composites on the hydrogen storage behavior of Mg₉₀Ce₅Y₅ alloy was investigated in detail by XRD SEM TEM PCI and DSC method. Because of the synergistic catalytic function of C and Co in C@Co nanocomposites the Mg₉₀Ce₅Y₅ alloy with 10 wt.% C@Co shows the excellent hydrogen absorption and desorption performances. Time for releasing hydrogen reduces from 150 min to 11 min with the addition of the C@Co composites at the temperature of 300 °C. Meanwhile the dehydrogenation activation energy also declines from 130.3 to 81.9 kJ mol−1 H₂ after the addition of the C@Co composites. This positive effect attributes to the C layer with the high defect density and the Co nanoparticles which reduces the energy barriers for the nucleation of Mg/MgH₂ phase and the recombination of hydrogen molecule. Besides the C@Co composites also improve the activation property of the Mg₉₀Ce₅Y₅ alloy which was fully activated in the first cycle. Moreover the temperature for initial dehydrogenation and the endothermic peak of the alloy hydride were also decreased. Although the addition of the C@Co composites increases the plateau pressures and decreases the value of the decomposition enthalpy these differences are so small that the improvement on thermodynamics can hardly be seen.