Saudi Arabia

The continuous rise of global carbon emissions demands the utilization of fossil fuels in a sustainable way. Owing to various forms of emissions our environment conditions might be affected necessitating more focus of scientists and researchers to upgrade oil processing to more efficient manner. Gasification is a potential technology that can convert fossil fuels to produce clean and environmentally friendly hydrogen fuel in an economical manner. Therefore this study analyzed and examined it critically. In this study two different routes for the production of high-purity hydrogen from vacuum residue while minimizing the carbon emissions were proposed. The first route (Case I) studied the gasification of heavy vacuum residue (VR) in series with dry methane reforming (DMR). The second route studied the gasification of VR in parallel integration with DMR (Case II). After investigating both processes a brief comparison was made between the two routes of hydrogen production in terms of their CO2 emissions energy efficiency energy consumption and environmental and economic impacts. In this study the two vacuum-residue-to-hydrogen (VRTH) processes were simulated using Aspen Plus for a hydrogen production capacity of 50 t/h with 99.9 wt.% purity. The results showed that Case II offered a process energy efficiency of 57.8% which was slightly higher than that of Case I. The unit cost of the hydrogen product for Case II was USD 15.95 per metric ton of hydrogen which was almost 9% lower than that of Case I. In terms of the environmental analysis both cases had comparably low carbon emissions of around 8.3 kg of CO2/kg of hydrogen produced; with such high purity the hydrogen could be used for production of other products further downstream or for industrial applications.

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.

Hydrogen (H₂) is a promising renewable energy source that can replace fossil fuels since it can solve several environmental and economic issues. However the widespread usage of H₂ is constrained by its storage and safety issues. Many researchers consider solid materials with an excellent capacity for H₂ storage and generation as the solution for most H₂-related issues. Among solid materials ammonia borane (abbreviated hereafter as AB) is considered one of the best hydrogen storage materials due to its extraordinary H₂ content and small density. However the process must be conducted in the presence of efficient catalysts to obtain a reasonable amount of generated H₂. Electrospun nanofibrous catalysts are a new class of efficient catalysts that involves the usage of polymers. Here a comprehensive review of the ceramic-supported electrospun NF catalysts for AB hydrolysis is presented with a special focus on catalytic and photolytic performance and preparation steps. Photocatalytic AB hydrolysis was discussed in detail due to its importance and promising results. AB photocatalytic hydrolysis mechanisms under light were also explained. Electrospun catalysts show excellent activity for AB hydrolysis with good recyclability. Kinetics studies show that the AB hydrolysis reaction is independent of AB concentration and the first-order reaction of NF catalysts.

This work reports on H2 fuel generation from sewage water using Cu/CuO nanoporous (NP) electrodes. This is a novel concept for converting contaminated water into H2 fuel. The preparation of Cu/CuO NP was achieved using a simple thermal combustion process of Cu metallic foil at 550 ◦C for 1 h. The Cu/CuO surface consists of island-like structures with an inter-distance of 100 nm. Each island has a highly porous surface with a pore diameter of about 250 nm. X-ray diffraction (XRD) confirmed the formation of monoclinic Cu/CuO NP material with a crystallite size of 89 nm. The prepared Cu/CuO photoelectrode was applied for H2 generation from sewage water achieving an incident to photon conversion efficiency (IPCE) of 14.6%. Further the effects of light intensity and wavelength on the photoelectrode performance were assessed. The current density (Jph) value increased from 2.17 to 4.7 mA·cm−2 upon raising the light power density from 50 to 100 mW·cm−2 . Moreover the enthalpy (∆H*) and entropy (∆S*) values of Cu/CuO electrode were determined as 9.519 KJ mol−1 and 180.4 JK−1 ·mol−1 respectively. The results obtained in the present study are very promising for solving the problem of energy in far regions by converting sewage water to H2 fuel.

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.

Natural gas pipelines have attracted increasing attention in the energy industry thanks to the current demand for green energy and the advantages of pipeline transportation. A novel deep learning method is proposed in this paper using a coupled network structure incorporating the thermodynamics-informed neural network and the compressor Boolean neural network to incorporate both functions of pipeline transportation safety check and energy supply predictions. The deep learning model is uniformed for the coupled network structure and the prediction efficiency and accuracy are validated by a number of numerical tests simulating various engineering scenarios including hydrogen gas pipelines. The trained model can provide dispatchers with suggestions about the number of phases existing during the transportation as an index showing safety while the effects of operation temperature pressure and compositional purity are investigated to suggest the optimized productions.

Photocatalysts lead vitally to water purifications and decarbonise environment each by wastewater treatment and hydrogen (H2 ) production as a renewable energy source from waterphotolysis. This work deals with the photocatalytic degradation of ciprofloxacin (CIP) and H2 production by novel silver-nanoparticle (AgNPs) based ternary-nanocomposites of thiolated reducegraphene oxide graphitic carbon nitride (AgNPs-S-rGO2%@g-C3N4 ) material. Herein the optimised balanced ratio of thiolated reduce-graphene oxide in prepared ternary-nanocomposites played matchlessly to enhance activity by increasing the charge carriers’ movements via slowing down charge-recombination ratios. Reduced graphene oxide (rGO) >2 wt.% or < 10 nm. Therefore AgNPs-S-rGO2%@g-C3N4 has 3772.5 µmolg−1 h −1 H2 production which is 6.43-fold higher than g-C3N4 having cyclic stability of 96% even after four consecutive cycles. The proposed mechanism for AgNPs-S-rGO2%@g-C3N4 revealed that the photo-excited electrons in the conduction-band of g-C3N4 react with the adhered water moieties to generate H2 .

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.

This study provides H2 gas as a renewable energy source from sewage water splitting reaction using a PMT/Au photocathode. So this study has a dual benefit for hydrogen generation; at the same time it removes the contaminations of sewage water. The preparation of the PMT is carried out through the polymerization process from an acid medium. Then the Au sputter was carried out using the sputter device under different times (1 and 2 min) for PMT/Au-1 min and PMT/Au-2min respectively. The complete analyses confirm the chemical structure such as XRD FTIR HNMR SEM and Vis-UV optical analyses. The prepared electrode PMT/Au is used for the hydrogen generation reaction using Na2S2O3 or sewage water as an electrolyte. The PMT crystalline size is 15 nm. The incident photon to current efficiency (IPCE) efficiency increases from 2.3 to 3.6% (at 390 nm) and the number of H2 moles increases from 8.4 to 33.1 mmol h−1 cm−2 for using Na2S2O3 and sewage water as electrolyte respectively. Moreover all the thermodynamic parameters such as activation energy (Ea) enthalpy (∆H*) and entropy (∆S*) were calculated; additionally a simple mechanism is mentioned for the water-splitting reaction.

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.