Saudi Arabia

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 As such storage of H2 in geological formations has been considered as a potential solution where it can be withdrawn again at the larger stage for utilization.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.

Of all the available resources given to mankind the sunlight is perhaps the most abundant renewable energy resource providing more than enough energy on earth to satisfy all the needs of humanity for several hundred years. Therefore it is transient and sporadic that poses issues with how the energy can be harvested and processed when the sun does not shine. Scientists assume that electro/photoelectrochemical devices used for water splitting into hydrogen and oxygen may have one solution to solve this hindrance. Water electrolysis-generated hydrogen is an optimal energy carrier to store these forms of energy on scalable levels because the energy density is high and no air pollution or toxic gas is released into the environment after combustion. However in order to adopt these devices for readily use they have to be low-cost for manufacturing and operation. It is thus crucial to develop electrocatalysts for water splitting based on low-cost and land-rich elements. In this review I will summarize current advances in the synthesis of low-cost earth-abundant electrocatalysts for overall water splitting with a particular focus on how to be linked with photoelectrocatalytic water splitting devices. The major obstacles that persist in designing these devices. The potential future developments in the production of efficient electrocatalysts for water electrolysis are also described.

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 future depends on large-scale storage which can be provided by geological formations (such as caverns aquifers and depleted oil and gas reservoirs) to handle demand and supply changes a typical hysteresis of most renewable energy sources. Amongst them depleted natural gas reservoirs are the most cost-effective and secure solutions due to their wide geographic distribution proven surface facilities and less ambiguous site evaluation. They also require less cushion gas as the native residual gases serve as a buffer for pressure maintenance during storage. However there is a lack of thorough understanding of this technology. This work aims to provide a comprehensive insight and technical outlook into hydrogen storage in depleted gas reservoirs. It briefly discusses the operating and potential facilities case studies and the thermophysical and petrophysical properties of storage and withdrawal capacity gas immobilization and efficient gas containment. Furthermore a comparative approach to hydrogen methane and carbon dioxide with respect to well integrity during gas storage has been highlighted. A summary of the key findings challenges and prospects has also been reported. Based on the review hydrodynamics geochemical and microbial factors are the subsurface’s principal promoters of hydrogen losses. The injection strategy reservoir features quality and operational parameters significantly impact gas storage in depleted reservoirs. Future works (experimental and simulation) were recommended to focus on the hydrodynamics and geomechanics aspects related to migration mixing and dispersion for improved recovery. Overall this review provides a streamlined insight into hydrogen storage in depleted gas reservoirs.

The present study investigates a process for the selective production of hydrogen from the catalytic decomposition of formic acid in the presence of iridium and iridium–palladium nanoparticles under various conditions. It was found that a loading of 1 wt.% of 2% palladium in the presence of 1% iridium over activated charcoal led to a 43% conversion of formic acid to hydrogen at room temperature after 4 h. Increasing the temperature to 60 °C led to further decomposition and an improvement in conversion yield to 63%. Dilution of formic acid from 0.5 to 0.2 M improved the decomposition reaching conversion to 81%. The reported process could potentially be used in commercial applications.

Although most of researchers agree on the elementary reactions behind the sonolytic formation of molecular hydrogen (H₂) from water namely the radical attack of H₂O and H₂O₂ and the free radicals recombination several recent papers ignore the intervention of the dissolved gas molecules in the kinetic pathways of free radicals and hence may wrongly assess the effect of dissolved gases on the sonochemical production of hydrogen. One may fairly ask to which extent is it acceptable to ignore the role of the dissolved gas and its eventual decomposition inside the acoustic cavitation bubble? The present opinion paper discusses numerically the ways in which the nature of dissolved gas i.e. N₂ O₂ Ar and air may influence the kinetics of sonochemical hydrogen formation. The model evaluates the extent of direct physical effects i.e. dynamics of bubble oscillation and collapse events if any against indirect chemical effects i.e. the chemical reactions of free radicals formation and consequently hydrogen emergence it demonstrates the improvement in the sonochemical hydrogen production under argon and sheds light on several misinterpretations reported in earlier works due to wrong assumptions mainly related to initial conditions. The paper also highlights the role of dissolved gases in the nature of created cavitation and hence the eventual bubble population phenomena that may prevent the achievement of the sonochemical activity. This is particularly demonstrated experimentally using a 20 kHz Sinaptec transducer and a Photron SA 5 high speed camera in the case of CO₂-saturated water where degassing bubbles are formed instead of transient cavitation.

Observing the growing energy demand of modern societies many countries have recognized energy security as a looming problem and renewable energies as a solution to this issue. Renewable hydrogen production is an excellent method for the storage and transfer of energy generated by intermittent renewable sources such as wind and solar so that they can be used at a place and time of our choosing. In this study the suitability of 15 cities in Fars province Iran for renewable hydrogen production was investigated and compared by the use of multiple multi-criteria decision-making methods including ARAS SAW CODAS and TOPSIS. The obtained rankings were aggregated by rank averaging Borda method and Copeland method. Finally the partially ordered set ranking technique was used to reach a general consensus about the ranking. The criteria that affect hydrogen production were found to be solar energy potential wind energy potential population air temperature natural disasters altitude relative humidity land cost skilled labor infrastructure topographic condition and distance from main roads. These criteria were weighted using the best–worst method (BWM) based on the data collected by a questionnaire. Solar energy potential was estimated using the Angstrom model. Wind energy potential was estimated by using the Weibull distribution function for each month independently. The results of the multi-criteria decision-making methods showed Izadkhast to be the most suitable location for renewable hydrogen production in the studied area.

Solutions that simulate hydrometallurgical base metal process streams with high nickel (Ni) and minor platinum (Pt) concentrations were used to create Pt/Ni nanoparticles on TiO₂ nanotube surfaces. For this electrochemical deposition – redox replacement (EDRR) was used that also allowed to control the nanoparticle size density and Pt/Ni content of the deposited nanoparticles. The Pt/Ni nanoparticle decorated titanium dioxide nanotubes (TiO₂ nanotubes) become strongly activated for photocatalytic hydrogen (H₂) evolution. Moreover EDRR facilitates nanoparticle formation without the need for any additional chemicals and is more effective than electrodeposition alone. Actually a 10000-time enrichment level of Pt took place on the TiO₂ surface when compared to Pt content in the solution with the EDRR method. The results show that hydrometallurgical streams offer great potential as an alternative raw material source for industrial catalyst production when coupled with redox replacement electrochemistry.

Feeding IC engines with hydrogen‐rich syngas as an admixture to hydrocarbon fuels can decrease pollutant emissions particularly NOx. It offers a potential technique for low‐environmen‐ tal impact hydrocarbon fuel use in automotive applications. However hydrogen‐rich reformate gas (syngas) production via fuel reforming still needs more research and optimization. In this paper we describe the effect of a plasma torch assembly design on syngas yield and composition during plasma‐assisted reforming of gasoline. Additionally erosion resistance of the cathode‐emitting ma‐ terial under the conditions of gasoline reforming was studied using hafnium metal and lanthanated tungsten alloy. The gasoline reforming was performed with a noncatalytic nonthermal low‐current plasma system in the conditions of partial oxidation in an air and steam mixture. To find the most efficient plasma torch assembly configuration in terms of hydrogen production yield four types of anode design were tested i.e. two types of the swirl ring and two cathode materials while varying the inlet air and fuel flow rates. The experimental results showed that hydrogen was the highest proportion of the produced syngas. The smooth funnel shape anode design in Ring 1 at air/fuel flow rates of 24/4 27/4.5 and 30/5 g/min respectively was more effective than the edged funnel shape. Lanthanated tungsten alloy displayed higher erosion resistance than hafnium metal.

Power ultrasonic (> 100 kHz) splits water into free radicals and hydrogen. As a result water sonochemistry is considered as an alternative clean and fossil-fuel-free hydrogen production technique. In this research work the impact of rare gases (Xe Ar and He) on the sonochemical production of hydrogen as well as the population of active bubbles has been investigated computationally for various sonicated frequencies (213-515 kHz) and intensities (1-2 W/cm²). It has been found that both the H2 yielding and the bubble population size for H2 yielding are in the order Xe>Ar>He whatever the imposed sonolytic parameters (i.e. frequency and power). These findings were principally ascribed to the thermal conductivity of the saturating gases which is in the reverse order (He>Ar>Xe). Besides the difference between Ar and Xe is condensed in comparison with the He gas. For wave frequencies larger than 213 kHz however all saturating gases (Xe Ar and He) behave identically with the influence of thermal conductivity of these gases on the optimal radius muted. At 213 kHz however this impact is plainly visible (Ropt (Ar and Xe)>Ropt (He)). As per the results obtained helium's inefficiency as a saturating gas for hydrogen production is verified but xenon's maximal efficacy is reached when water is saturated with it. These results support the fewer experimental data reported in this emerging branch of sonochemistry while the discussed results in the present (i.e. noble gases effect on sono-hydrogen production) are treated for the first time consequently our work is considered as a guideline for increasing the efficacy of hydrogen production in a sonochemical reactor.