An active direction control method in rotating detonation combustor

rotating direction of detonation waves is one of the essential characteristics of the unsteady flow fields in the rotating detonation combustors (RDCs). However, it changes over time and is challenging to predict. Pre-detonator is commonly used to initiate the RDC in experiments. Intuitively, the detonation wave should continue in the direction of the pre-detonator. Unfortunately, experimental results often contradict this expectation. Three-dimensional numerical simulations of a rotating detonation combustor installed with a pre-detonator are performed in the present study. The numerical experiments show that the pre-detonator induces two counter-rotating detonation waves in the annular chamber and fails in fixed-direction initiation. Furthermore, we propose an active direction control method in the present study. This method utilizes the pre-detonator as a control device and successfully regulates the detonation waves along the pre-detonator direction. The active direction control method allows adjusting the propagating direction of detonation waves anytime during the RDC operation. By this method, multiple waves tend to be produced in the flow field, enhancing the stability of the rotating detonation combustor.     

Transition to detonation in a hydrogen-air mixtures due to shock wave focusing in the 90 - deg corner

This work presents experimental observation of the ignition modes due to shock wave focusing in a 90 - deg corner in a mixture of 20%–55% H₂ in air with the main purpose of recognizing critical conditions for transition to detonation. The results showed three ignition modes, first ‘weak’ ignition followed by deflagration with ignition delay time higher than ∼1 μs, second ‘strong’ with instantaneous transition to detonation, and third with deflagrative ignition and delayed transition to detonation. The transition was observed only when specific shock wave velocity was reached. The transition velocity for stoichiometric mixture was approx. 715 m/s corresponding to M = 1.75 and 71% of speed of sound in products. For leaner or richer mixtures, the transition velocity increased approaching the speed of sound in products at approx. 18% and 58% H₂.     

Evaluation of performance characteristics of a novel hydrogen-fuelled free-piston engine generator

In this work, we present the experimental results obtained from hydrogen fuelled spark-ignited dual piston free-piston engine generator (FPEG) prototype operated in two-stroke and four-stroke mode. The FPEG testing was successfully conducted at 3.7 compression ratio, engine speed between 5 Hz and 11 Hz and with different equivalence ratios. The FPEG technical details, experimental set-up and operational control are explained in detail. Performance indicators show that both equivalence ratio and engine speed affect the engine operation characteristics. For every set of specified FPEG parameters, appropriate range of equivalence ratio is recommended to prevent unwanted disturbance to electric generator operation. Both two-stroke and four-stroke cycle mode were tested, and the results showed different combustion characteristics with the two thermodynamic cycles. Four-stroke cycle mode could operate with indicated thermal efficiency gain up to 13.2% compared with the two-stroke cycle.     

Multi-state techno-economic model for optimal dispatch of grid connected hydrogen electrolysis systems operating under dynamic conditions

The production of hydrogen through water electrolysis is a promising pathway to decarbonize the energy sector. This paper presents a techno-economic model of electrolysis plants based on multiple states of operation: production, hot standby and idle. The model enables the calculation of the optimal hourly dispatch of electrolyzers to produce hydrogen for different end uses. This model has been tested with real data from an existing installation and compared with a simpler electrolyzer model that is based on two states. The results indicate that an operational strategy that considers the multi-state model leads to a decrease in final hydrogen production costs. These reduced costs will benefit businesses, especially while electrolysis plants grow in size to accommodate further increases in demand.     

Recent advances in artificial neural network research for modeling hydrogen production processes

Artificial Neural Networks (ANN) have been widely used by scientists in a variety of energy modes (biomass, wind, solar, geothermal, and hydroelectric). This review highlights the assistance of ANN for researchers in the quest for discovering more advanced materials/processes for efficient hydrogen production (HP). The review is divided into two parts in this context. The first section briefly mentions, in terms of technologies, economy, energy consumption, and costs symmetrically outlined the advantages and disadvantages of various HP routes such as fossil fuel/biomass conversion, water electrolysis, microbial fermentation, and photocatalysis. Subsequently, ANN and ANN hybrid studies implemented in HP research were evaluated. Finally, statistics of hybrid studies with ANN are given, and future research proposals and hot research topics are briefly discussed. This research, which touches upon the types of ANNs applied to HP methods and their comparison with other modeling techniques, has an essential place in its field.     

Variations of methane conversion process with the geometrical effect in rotating gliding arc reactor

Controllability of the kinetic path of methane conversion in plasma driven oxidation reaction is investigated. Different geometries in a rotating gliding arc reactor are adopted to control reaction paths in methane oxidation reaction. Diverging and converging type reactor product different reaction environments in view point of both the reaction time and the degree of thermal activation. In the diverging reactor, the partial oxidation process is dominant with high methane conversion because the diverging section facilitates to elongate the arc length and decrease the flow velocity. Thus, the convective and radiative heat transfer from the arc column to the reactants could be enhanced. The role of plasma in the diverging reactor is mainly igniting and sustaining the partial oxidation, which is rather different from that in the converging reactor where the plasma plays as a heat source for thermal pyrolysis of methane with the help of focusing thermal energy of the arc.     

Simultaneous biohydrogen (H2) and bioplastic (poly-β-hydroxybutyrate-PHB) productions under dark,photo, and subsequent dark and photo fermentation utilizing various wastes

The present study is focused on bio hydrogen (H₂) and bioplastic (i.e., poly-β-hydroxybutyrate; PHB) productions utilizing various wastes under dark fermentation, photo fermentation and subsequent dark-photo fermentation. Potential bio H₂ and PHB producing microbes were enriched and isolated. The effects of substrate (rice husk hydrolysate, rice straw hydrolysate, dairy industry wastewater, and rice mill wastewater) concentration (10–100%) and pH (5.5–8.0) were examined in the batch mode under the dark and photo fermentation conditions. Using 100% rice straw hydrolysate at pH 7, the maximum bio H₂ (1.53 ± 0.04 mol H₂/mol glucose) and PHB (9.8 ± 0.14 g/L) were produced under dark fermentation condition by Bacillus cereus. In the subsequent dark-photo fermentation, the highest amounts of bio H₂ and PHB were recorded utilizing 100% rice straw hydrolysate (1.82 ± 0.01 mol H₂/mol glucose and 19.15 ± 0.25 g/L PHB) at a pH of 7.0 using Bacillus cereus (KR809374) and Rhodopseudomonas rutila. The subsequent dark-photo fermentative bio H₂ and PHB productions obtained using renewable biomass (i.e., rice husk hydrolysate and rice straw hydrolysate) can be considered with respect to the sustainable management of global energy sources and environmental issues.     

Molten salt synthesis of high-entropy alloy AlCoCrFeNiV nanoparticles for the catalytic hydrogenation of p-nitrophenol by NaBH4

High-entropy alloy (HEA) AlCoCrFeNiV nanoparticles were prepared from oxide precursors using a molten salt synthesis method without an electrical supply. The oxide precursor was directly reduced by CaH₂ reducing agent in molten LiCl at 600°C-700°C or molten LiCl–CaCl₂ at 500°C-550°C. When the reduction was conducted at 700°C, a face-centered cubic (FCC) structure produced, as identified by X-ray diffraction analysis. With lower reduction temperatures, the FCC structure was absent, replaced by a body-centered cubic (BCC) structure. With a reduction temperature of 550°C, the resulting sample was composed of highly pure HEA AlCoCrFeNiV nanoparticles with a BCC structure of 15 nm. Analyses by scanning electron microscopy/transmission electron microscopy with energy-dispersive X-ray spectroscopy confirmed the formation of homogeneous HEA AlCoCrFeNiV with a nanoscale morphology. In the hydrogenation reaction of p-nitrophenol by NaBH₄, the AlCoCrFeNiV nanoparticles (produced at 550°C) exhibited a catalytic activity with ～90% conversion and 16 kJ/mol activation energy.     

Hydrogen-powered vehicles for autonomous ride-hailing fleets

Autonomous ride-hailing fleets are approaching commercialization as an on-demand, low-cost transportation solution. Although battery electric vehicles (BEVs) are well-studied for this application, hydrogen fuel cell electric vehicles (FCEVs) may provide additional advantages that have not been sufficiently investigated. Here, we developed a stochastic ride-hailing autonomous vehicle (RHAV) model to compare these technologies and applied this model to seven BEVs and two FCEVs. FCEV fleets are 3–10% smaller than BEV fleets due to shorter refueling times and greater driving ranges, which enable greater fleet efficiency. The Hyundai Kona (BEV) provides the greatest fleet profitability; however, the Toyota Mirai (FCEV) is only 3% less profitable despite having a 25% higher purchase price. We demonstrate that FCEVs are economically competitive as RHAVs, and that expected price reductions can make them the most profitable technology. Furthermore, FCEV fleets provide qualitative benefits, including a substantial increase in local hydrogen demand to catalyze hydrogen infrastructure development.     

Kinetics of formic acid decomposition in subcritical and supercritical water – a Raman spectroscopic study

The decomposition of formic acid is studied in a continuous sub- or supercritical water reactor at temperatures between 300 and 430 °C, a pressure of 25 MPa, residence times between 4 and 65 s, and a feedstock concentration of 3.6 wt%. In situ Raman spectroscopy is used to produce real-time data and accurately quantify decomposition product yields of H₂, CO₂, and CO. Collected spectra are used to determine global decomposition rates and kinetic rates for individual reaction pathways. First-order global Arrhenius parameters are determined as log A (s⁻¹) = 1.6 ± 0.20 and E_A = 9.5 ± 0.55 kcal/mol for subcritical decomposition, and log A (s⁻¹) = 12.56 ± 1.96 and E_A = 41.90 ± 6.08 kcal/mol for supercritical decomposition. Subcritical and supercritical Arrhenius parameters for individual pathways are proposed. The variance in rate parameters is likely due to changing thermophysical properties of water across the critical point. There is strong evidence for a surface catalyzed free-radical mechanism responsible for rapid decomposition above the critical point, facilitated by low density at supercritical conditions.     

Hydrofluoroolefin-based mixed refrigerant for enhanced performance of hydrogen liquefaction process

Hydrogen has the highest gravimetric energy density of all fuels; however, it has a low volumetric energy density, unfavorable for storage and transportation. Hydrogen is usually liquefied to meet the bulk transportation needs. The exothermic interconversion of its spin isomers is an additional activity to an already energy-intensive process. The most significant temperature drop occurs in the precooling cycle (between ?150 °C and up to ?180 °C) and consumes more than 50% of the required energy. To reduce the energy consumption and improve the exergy efficiency of the hydrogen liquefaction process, a new high-boiling component, Hydrofluoroolefin (HFO-1234yf), is added to the precooled mixed refrigerant. As a result, the specific energy consumption of precooling cycle reduces by 41.8%, from 10.15 kWh/kg_LH2 to 5.90 kWh/kg_LH2, for the overall process. The exergy efficiency of the proposed case increases by 43.7%; however, the total equipment cost is also the highest. The inflated cost is primarily due to the added ortho-to-para hydrogen conversion reactor, boosting the para-hydrogen concentration. From the perspective of bulk storage and transportation of liquid hydrogen, the simplicity of design and low energy consumption build a convincing case for considering the commercialization of the process.     

Power flow control of grid connected hybrid renewable energy system using hybrid controller with pumped storage

This paper presents a grid-connected HRES using a hybrid controller with PHS for optimal power flow control and minimizing the production cost. The novelty of the proposed approach is the joined execution of the SSA and CSA named as SSA-CS are apparently a very new metaheuristic algorithm. Moreover, the proposed method is the cost-effective power production of the microgrids and effective utilization of renewable energy sources without wasting the available energy. Here, the energy sources in particular PV system, WT, MT and battery with PHS are utilized to generate the power of the MG system. In the proposed approach, the required power demand of the energy system is predicted by the ANN technique. After that, the production cost minimization is done in view of the anticipated load demand by utilizing the optimization approaches to be a specific SSA-CS algorithm. The result of the proposed approach is actualized in the MATLAB/Simulink working platform. The performance of the proposed approach is examined by comparing the current methodologies such as SSA and PSO with the proposed SSA-CS approach. The simulation results show that the proposed method generates maximum power and furthermore the proposed framework has less production cost in light of the power demand.     

CoMo heterohierarchical foam-structured cathode for anion exchange membrane water electrolyzer

It is important to consider the synergy of heterostructures to improve the slow kinetics of water dissociation in the alkaline hydrogen evolution reaction (HER). Herein, we report a simple method to design a heterohierarchical CoMo catalyst. The CoMo catalyst was prepared by simple one-pot electrodeposition on carbon paper (CP). The CoMo/CP catalyst was optimized for the alkaline HER by controlling the electrodeposition bath conditions, potential, and time. The optimized catalyst shows the heterohierarchical structure containing the electrically conductive metallic Co in the bulk and Mo-incorporated Co containing Mo⁴⁺ at the surface. It exhibited a lower HER overpotential of 0.11 V at ?20 mA/cm² compared to those of the others owing to the synergetic effect of the between the Co and Mo incorporated Co. The results highlight the advantages of the simple method developed herein for the design of heterohierarchical catalysts.     

Improving inter-plant integration of syngas production technologies by the recycling of CO2 and by-product of the Fischer-Tropsch process

This paper deals with the emission reduction in synthesis-gas production by better integration and increasing the energy efficiency of a high-temperature co-electrolysis unit combined with the Fischer-Tropsch process. The investigated process utilises the by-product of Fischer-Tropsch, as an energy source and carbon dioxide as a feedstock for synthesis gas production. The proposed approach is based on adjusting process streams temperatures with the further synthesis of a new heat exchangers network and optimisation of the utility system. The potential of secondary energy resources was determined using plus/minus principles and simulation of a high-temperature co-electrolysis unit. The proposed technique maximises the economic and environmental benefits of inter-unit integration. Two scenarios were considered for sharing the high-temperature co-electrolysis and the Fischer-Tropsch process. In the first scenario, by-products from the Fischer-Tropsch process were used as fuel for a high-temperature co-electrolysis. Optimisation of secondary energy sources and the synthesis of a new heat exchanger network reduce fuel consumption by 47% and electricity by 11%. An additional environmental benefit is reflected in emission reduction by 25,145 tCO₂/y. The second scenario uses fossil fuel as a primary energy source. The new exchanger network for the high-temperature co-electrolysis was built for different energy sources. The use of natural gas resulted in total annual costs of the heat exchanger network to 1,388,034 USD/y, which is 1%, 14%, 116% less than for coal, fuel oil and LPG, respectively. The use of natural gas as a fuel has the lowest carbon footprint of 7288 tCO₂/y. On the other hand, coal as an energy source has commensurable economic indicators that produce 2 times more CO₂, which can be used as a feedstock for a high-temperature co-electrolysis. This work shows how in-depth preliminary analysis can optimise the use of primary and secondary energy resources during inter-plant integration.     

Determination of the potential of cyanobacterial strains for hydrogen production

Hydrogen (H₂) is a renewable, abundant, and nonpolluting source of energy. Photosynthetic organisms capture sunlight very efficiently and convert it into organic molecules. Cyanobacteria produce H₂ by breaking down organic compounds and water. In this study, biological H₂ was produced from various strains of cyanobacteria. Moreover, H₂ accumulation by Synechocystis sp. PCC 6803 was as high as 0.037 μmol/mg Chl/h within 120 h in the dark. The wild-type, filamentous, non-heterocystous cyanobacterium Desertifilum sp. IPPAS B-1220 was found to produce a maximum of 0.229 μmol/mg Chl/h in the gas phase within 166 h in the light, which was on par with the maximum yield reported in the literature. DCMU at 10 μM increased H₂ production by Desertifilum sp. IPPAS B-1220 by 1.5-fold to 0.348 μmol H₂/mg Chl/h. This is the first report on the capability of Desertifilum cyanobacterium to produce H₂.     

HRT control as a strategy to enhance continuous hydrogen production from sugarcane juice under mesophilic and thermophilic conditions in AFBRs

The objective of this study was to evaluate the effects of hydraulic retention time (HRT) (8–1 h) on H₂ production from sugarcane juice (5000 mg COD L⁻¹) in mesophilic (30 °C, AFBR-30) and thermophilic (55 °C, AFBR-55) anaerobic fluidized bed reactors (AFBRs). At HRTs of 8 and 1 h in AFBR-30, the H₂ production rates were 60 and 116 mL H₂ h⁻¹ L⁻¹, the hydrogen yields were 0.60 and 0.10 mol H₂ mol⁻¹ hexose, and the highest bacterial diversities were 2.47 and 2.34, respectively. In AFBR-55, the decrease in the HRT from 8 to 1 h increased the hydrogen production rate to 501 mL H₂ h⁻¹ L⁻¹ at the HRT of 1 h. The maximum hydrogen yield of 1.52 mol H₂ mol⁻¹ hexose was observed at the HRT of 2 h and was associated with the lowest bacterial diversity (0.92) and highest bacterial dominance (0.52).     

Biomass gasification coupled with producer gas cleaning,bottling and HTS catalyst treatment for H2-rich gas production

The aim of the present study is to demonstrate the production of hydrogen-rich fuel gas from J. curcas residue cake. A comprehensive experimental study for the production of hydrogen rich fuel gas from J. curcas residue cake via downdraft gasification followed by high temperature water gas shift catalytic treatment has been carried out. The gasification experiments are performed at different equivalence ratios and performance of the process is reported in terms of producer gas composition & its calorific value, gas production rate and cold gas efficiency. The producer gas is cleaned of tar and particulate matters by passing it through venturi scrubber followed by sand bed filter. The clean producer gas is then compressed at 0.6 MPa and bottled into a gas cylinder. The bottled producer gas and a simulated mixture of producer gas are then subjected to high temperature shift (HTS) catalytic treatment for hydrogen enriched gas production. The effect of three different operating parameters GHSV, steam to CO ratio and reactor temperature on the product gas composition and CO conversion is reported. From the experimental study it is found that, the presence of oxygen in the bottled producer gas has affected the catalyst activity. Moreover, higher concentration of oxygen concentration in the bottled producer gas leads to the instantaneous deactivation of the HTS catalyst.     

Thermophysical properties of the liquid organic hydrogen carrier system based on diphenylmethane with the byproducts fluorene or perhydrofluorene

Fluorene (H0-F) and perhydrofluorene (H12-F) represent process-related byproducts formed by a dehydrocyclization step in the liquid organic hydrogen carrier (LOHC) system based on diphenylmethane (H0-DPM) and dicyclohexylmethane (H12-DPM). The influence of these byproducts on the liquid viscosity, surface tension, and liquid density of the DPM-based system was experimentally determined by studying three dehydrogenated binary mixtures with H0-F mole fractions of 0.05, 0.10, and 0.20 as well as one hydrogenated binary mixture with an H12-F mole fraction of 0.10 close to 0.1 MPa from (283–573) K. The densities increase with increasing share of H0-F or H12-F by around 1% per added byproduct mole fraction of 0.1. For the surface tension, an increase relative to the values of H0-DPM or H12-DPM by up to 6% is found. The addition of H0-F to H0-DPM or H12-F to H12-DPM yields a relative increase in viscosity by up to 9% at the lowest temperature studied.