China, People’s Republic

Direct CO₂ hydrogenation to hydrocarbons is a promising method of reducing CO2 emissions along with producing value-added products. However reactor design and performance have remained a challenging issue because of low olefin efficiency and high water production as a by-product. Accordingly a one-dimensional non-isothermal mathematical model is proposed to predict the membrane reactor performance and statistical analysis is used to assess the effects of important variables such as temperatures of reactor (Tr:A) shell (Ts:B) and tube (Tt:C) as well as sweep ratio (θ:D) and pressure ratio (φ:E) and their interactions on the products yields. In addition the optimized operating conditions are also obtained to achieve maximum olefin yields. Results reveal that interacting effects comprising AB (TrTs) AC (TrTt) AE (Trφ) BC (TsTt) CE (Ttφ) CD (Ttθ) and DE (θφ) play important roles on the product yields. It is concluded that higher temperatures at low sweep and pressure ratios can maximize the yields of olefins while simultaneously the yields of paraffins are minimized. In this regard optimized values for Tr Ts Tt θ and φ are determined as 325 °C 306.96 °C 325 °C 1 and 1 respectively.

Interactions between incident electromagnetic energy and matter are of critical importance for numerous civil and military applications such as photocatalysis solar cells optics radar detection communications information processing and transport et al. Traditional mechanisms for such interactions in the microwave frequency mainly rely on dipole rotations and magnetic domain resonance. In this study we present the first report of the microwave absorption of Al/H₂ treated TiO₂ nanoparticles where the Al/H₂ treatment not only induces structural and optical property changes but also largely improves the microwave absorption performance of TiO₂ nanoparticles. Moreover the frequency of the microwave absorption can be finely controlled with the treatment temperature and the absorption efficiency can reach optimal values with a careful temperature tuning. A large reflection loss of −58.02 dB has been demonstrated with 3.1 mm TiO₂ coating when the treating temperature is 700 °C. The high efficiency of microwave absorption is most likely linked to the disordering-induced property changes in the materials. Along with the increased microwave absorption properties are largely increased visible-light and IR absorptions and enhanced electrical conductivity and reduced skin-depth which is likely related to the interfacial defects within the TiO₂ nanoparticles caused by the Al/H₂ treatment.

Adjusting the structure of g-C₃N₄ to significantly enhance its photocatalytic activity has attracted considerable attention. Herein a novel sponge-like g-C₃N₄ with a porous structure is prepared from the annealing of protonated melamine under N2/H₂ atmosphere (PH-CN). Compared to bulk g-C₃N₄ via calcination of melamine under ambient atmosphere (B-CN) PH-CN displays thinner nanosheets and a higher surface area (150.1 m²/g) which is a benefit for shortening the diffusion distance of photoinduced carriers providing more active sites and finally favoring the enhancement of the photocatalytic activity. Moreover it can be clearly observed from the UV-vis spectrum that PH-CN displays better performance for harvesting light compared to B-CN. Additionally the PH-CN is prepared with a larger band gap of 2.88 eV with the Fermi level and conduction band potential increased and valence band potential decreased which could promote the water redox reaction. The application experiment results show that the hydrogen evolution rate on PH-CN was nearly 10 times higher than that of B-CN which was roughly 4104 μmol h⁻¹ g⁻¹. The method shown in this work provides an effective approach to adjust the structure of g-C₃N₄with considerable photocatalytic hydrogen evolution activity.

Densified liquid hydrogen/liquid oxygen is a promising propulsion fuel in the future. In order to systematically demonstrate the benefits and challenges of densified liquid hydrogen/liquid oxygen a transient thermodynamical model considering the heat leakage temperature rise engine thrust pressurization pressure of the tank and wall thickness of tank is developed in the present paper and the performance of densified liquid hydrogen/liquid oxygen as propulsion fuel is further evaluated in actual application. For liquid hydrogen/liquid oxygen tanks at different structural dimensions the effects of many factors such as temperature rise during propellant ground parking lift of engine thrust mass reduction of the tank structure and extension of spacecraft in‐orbit time are analyzed to demonstrate the comprehensive performance of liquid hydrogen/liquid oxygen after densification. Meanwhile the problem of subcooling combination matching of liquid hydro‐ gen/liquid oxygen is proposed for the first time. Combining the fuel consumption and engine thrust lifting the subcooling combination matching of liquid hydrogen/liquid oxygen at different mixing ratios and constant mixing ratios are discussed respectively. The results show that the relative engine thrust enhances by 6.96% compared with the normal boiling point state in the condition of slush hydrogen with 50% solid content and enough liquid oxygen. The in‐orbit time of spacecraft can extend about 2–6.5 days and 24–95 days for slush hydrogen with 50% solid content and liquid oxygen in the triple point state in different cryogenic tanks respectively. Due to temperature rise during parking the existing adiabatic storage scheme and filling scheme for densification LH2 need to be redesigned and for densification LO2 are suitable. It is found that there is an optimal subcooling matching relation after densification of liquid hydrogen/liquid oxygen as propulsion fuel. In other words the subcooling temperature of liquid hydrogen/liquid oxygen is not the lower the bet‐ ter but the matching relationship between LH2 subcooling degree and LO2 subcooling degree needs to be considered at the same time. It is necessary that the LO2 was cooled to 69.2 K and 54.5 K when the LH2 of 13.9 K and SH2 with 45% was adopted respectively. This research provides theoretical support for the promotion and application of densification cryogenic propellants.

Managing the concentration of atmospheric CO₂ requires a multifaceted engineering strategy which remains a highly challenging task. Reducing atmospheric CO₂ (CO2R) by converting it to value-added chemicals in a carbon neutral footprint manner must be the ultimate goal. The latest progress in CO2R through either abiotic (artificial catalysts) or biotic (natural enzymes) processes is reviewed herein. Abiotic CO2R can be conducted in the aqueous phase that usually leads to the formation of a mixture of CO formic acid and hydrogen. By contrast a wide spectrum of hydrocarbon species is often observed by abiotic CO2R in the gaseous phase. On the other hand biotic CO2R is often conducted in the aqueous phase and a wide spectrum of value-added chemicals are obtained. Key to the success of the abiotic process is understanding the surface chemistry of catalysts which significantly governs the reactivity and selectivity of CO2R. However in biotic CO2R operation conditions and reactor design are crucial to reaching a neutral carbon footprint. Future research needs to look toward neutral or even negative carbon footprint CO2R processes. Having a deep insight into the scientific and technological aspect of both abiotic and biotic CO2R would advance in designing efficient catalysts and microalgae farming systems. Integrating the abiotic and biotic CO2R such as microbial fuel cells further diversifies the spectrum of CO2R.

The current evidential effect of carbon emissions has become a societal challenge and the need to transition to cleaner energy sources/technologies has attracted wide research attention. Technologies that utilize low-grade heat like the organic Rankine cycle (ORC) and Kalina cycle have been proposed as viable approaches for fossil reduction/carbon mitigation. The development of renewable energy-based multigeneration systems is another alternative solution to this global challenge. Hence it is important to monitor the development of multigeneration energy systems based on low-grade heat. In this study a review of the ORC’s application in multigeneration systems is presented to highlight the recent development in ORC integrality/application. Beyond this a new ORC-CPVT (concentrated photovoltaic/thermal) integrated multigeneration system is also modeled and analyzed using the thermodynamics approach. Since most CPVT systems integrate hot water production in the thermal stem the proposed multigeneration system is designed to utilize part of the thermal energy to generate electricity and hydrogen. Although the CPVT system can achieve high energetic and exergetic efficiencies while producing thermal energy and electricity these efficiencies are 47.9% and 37.88% respectively for the CPVT-ORC multigeneration configuration. However it is noteworthy that the electricity generation from the CPVT-ORC configuration in this study is increased by 16%. In addition the hot water cooling effect and hydrogen generated from the multigeneration system are 0.4363 L/s 161 kW and 1.515 L/s respectively. The environmental analysis of the system also shows that the carbon emissions reduction potential is enormous.

Proton conducting SmNiO₃ (SNO) thin films were grown on (001) LaAlO₃ substrates for systematically investigating the proton transport properties. X-ray Diffraction and Atomic Force Microscopy studies reveal that the as-grown SNO thin films have good single crystallinity and smooth surface morphology. The electrical conductivity measurements in air indicate a peak at 473 K in the temperature dependence of the resistance of the SNO films probably due to oxygen loss on heating. A Metal-Insulator-Transition occurs at 373 K for the films after annealing at 873 K in air. In a hydrogen atmosphere (3% H2/97% N₂) an anomalous peak in the resistance is found at 685 K on the first heating cycle. Electrochemical Impedance Spectroscopy studies as a function of temperature indicate that the SNO films have a high ionic conductivity (0.030 S/cm at 773 K) in a hydrogen atmosphere. The activation energy for proton conductivity was determined to be 0.23 eV at 473–773 K and 0.37 eV at 773–973 K respectively. These findings demonstrate that SNO thin films have good proton conductivity and are good candidate electrolytes for low temperature proton-conducting Solid Oxide Fuel Cells.

A flake is a crack that is induced by trapped hydrogen within steel. To study its formation mechanism previous studies mostly focused on the formation process and magnitude of hydrogen pressure in hydrogen traps such as cavities and cracks. However according to recent studies the hydrogen leads to the decline of the mechanical properties of steel which is known as hydrogen embrittlement is another reason for flake formation. In addition the phenomenon of stress induced hydrogen uphill diffusion should not be neglected. All of the three behaviors are at work simultaneously. In order to further explore the formation mechanism of flakes in steel the process of flake initiation and growth were studied with the following three coupling factors: trap hydrogen pressure hydrogen embrittlement and stress induced hydrogen re-distribution. The analysis model was established using the finite element method and a crack whose radius is 0.5 mm was set in its center. The cohesive method and Bilinear Traction Separate Law (BTSL) were used to address the coupling effect. The results show that trap hydrogen pressure is the main driving force for flake formation. After the high hydrogen pressure was generated around the trap a stress field formed. In addition the trap is the center of stress concentration. Then hydrogen is concentrated in a distribution around this trap and most of the steel mechanical properties are reduced. The trap size is a key factor for defining the critical hydrogen content for flake formation and propagation. However when the trap size exceeds the specified value the critical hydrogen content does not change any more. As for the crack whose radius is 0.5 mm the critical hydrogen content of Cr5VMo steel is 2.2 ppm which is much closer to the maximum safe hydrogen concentration of 2.0 ppm used in China. The work presented in this article increases our understanding of flake formation and propagation mechanisms in steel.

The ever-increasing demand for energy coupled with dwindling fossil fuel resources make the establishment of a clean and sustainable energy system a compelling need. Hydrogen-based energy systems offer potential solutions. Although in the long-term the ultimate technological challenge is large-scale hydrogen production from renewable sources the pressing issue is how to store hydrogen efficiently on board hydrogen fuel-cell vehicles.

The study on temper embrittlement and hydrogen embrittlement of a test block from a 3Cr1Mo1/4V hydrogenation reactor after ten years of service was carried out by small punch test (SPT) at different temperatures. The SPT fracture energy Esp (derived from integrating the load-displacement curve) divided by the maximum load (Fm) of SPT was used to fit the Esp/Fm versus-temperature curve to determine the energy transition temperature (Tsp) which corresponded to the ductile-brittle transition temperature of the Charpy impact test. The results indicated that the ratio of Esp/Fm could better represent the energy of transition in SPT compared with Esp. The ductile-to-brittle transition temperature of the four different types of materials was measured using the hydrogen charging test by SPT. These four types of materials included the base metal and the weld metal in the as-received state and the base metal and the weld metal in the de-embrittled state. The results showed that there was a degree of temper embrittlement in the base metal and the weld metal after ten years of service at 390 °C. The specimens became slightly more brittle but this was not obvious after hydrogen charging. Because the toughness of the material of the hydrogenation reactor was very good the flat samples of SPT could not characterize the energy transition temperature within the liquid nitrogen temperature. Additionally there was no synergetic effect of temper embrittlement and hydrogen embrittlement found in 3Cr1Mo1/4V steel.

The grand challenges in renewable energy lie in our ability to comprehend efficient energy conversion systems together with dealing with the problem of intermittency via scalable energy storage systems. Relatively little progress has been made on this at grid scale and two overriding challenges still need to be addressed: (i) limiting damage to the environment and (ii) the question of environmentally friendly energy conversion. The present review focuses on a novel route for producing hydrogen the ultimate clean fuel from the Sun and renewable energy source. Hydrogen can be produced by light-driven photoelectrochemical (PEC) water splitting but it is very inefficient; rather we focus here on how electric fields can be applied to metal oxide/water systems in tailoring the interplay with their intrinsic electric fields and in how this can alter and boost PEC activity drawing both on experiment and non-equilibrium molecular simulation.

Globally the accelerating use of renewable energy sources enabled by increased efficiencies and reduced costs and driven by the need to mitigate the effects of climate change has significantly increased research in the areas of renewable energy production storage distribution and end-use. Central to this discussion is the use of hydrogen as a clean efficient energy vector for energy storage. This review by experts of Task 32 “Hydrogen-based Energy Storage” of the International Energy Agency Hydrogen TCP reports on the development over the last 6 years of hydrogen storage materials methods and techniques including electrochemical and thermal storage systems. An overview is given on the background to the various methods the current state of development and the future prospects. The following areas are covered; porous materials liquid hydrogen carriers complex hydrides intermetallic hydrides electro-chemical storage of energy thermal energy storage hydrogen energy systems and an outlook is presented for future prospects and research on hydrogen-based energy storage

Offshore oil and gas field development consumes quantities of electricity which is usually provided by gas turbines. In order to alleviate the emission reduction pressure and the increasing pressure of energy saving governments of the world have been promoting the reform of oil and gas fields for years. Nowadays environmentally friendly alternatives to provide electricity are hotspots such as the integration of traditional energy and renewable energy. However the determination of system with great environmental and economic benefits is still controversial. This paper proposed a wind– hydrogen–natural gas nexus (WHNGN) system for sustainable offshore oil and gas fields development. Combining the optimization model with the techno-economic evaluation model a comprehensive evaluation framework is established for techno-economic feasibility analysis. In addition to WHNGN system another two systems are designed for comparison including the traditional energy supply (TES) system and wind–natural gas nexus (WNGN) system. An offshore production platforms in Bohai Bay in China is taken as a case and the results indicate that: (i) WNGN and WHNGN systems have significant economic benefits total investment is decreased by 5190 and 5020 million $ respectively and the WHNGN system increases 4174 million $ profit; (ii) WNGN and WHNGN systems have significant environmental benefits annual carbon emission is decreased by 15 and 40.2 million kg respectively; (iii) the system can be ranked by economic benefits as follows: WHNGN >WNGN > TES; and (iV) the WHNGN system is more advantageous in areas with high hydrogen and natural gas sales prices such as China Kazakhstan Turkey India Malaysia and Indonesia.

The current hydrogen generation technologies especially biomass gasification using fluidized bed reactors (FBRs) were rigorously reviewed. There are involute operational parameters in a fluidized bed gasifier that determine the anticipated outcomes for hydrogen production purposes. However limited reviews are present that link these parametric conditions with the corresponding performances based on experimental data collection. Using the constructed artificial neural networks (ANNs) as the supervised machine learning algorithm for data training the operational parameters from 52 literature reports were utilized to perform both the qualitative and quantitative assessments of the performance such as the hydrogen yield (HY) hydrogen content (HC) and carbon conversion efficiency (CCE). Seven types of operational parameters including the steam-to-biomass ratio (SBR) equivalent ratio (ER) temperature particle size of the feedstock residence time lower heating value (LHV) and carbon content (CC) were closely investigated. Six binary parameters have been identified to be statistically significant to the performance parameters (hydrogen yield (HY)) hydrogen content (HC) and carbon conversion efficiency (CCE) by analysis of variance (ANOVA). The optimal operational conditions derived from the machine leaning were recommended according to the needs of the outcomes. This review may provide helpful insights for researchers to comprehensively consider the operational conditions in order to achieve high hydrogen production using fluidized bed reactors during biomass gasification.

Automobile exhaust heat recovery is considered to be an effective means to enhance fuel utilization. The catalytic production of hydrogen by methanol steam reforming is an attractive option for onboard mobile applications due to its many advantages. However the reformers of conventional packed bed type suffer from axial temperature gradients and cold spots resulting from severe limitations of mass and heat transfer. These disadvantages limit reformers to a low efficiency of catalyst utilization. A novel rib microreactor was designed for the hydrogen production from methanol steam reforming heated by automobile exhaust and the effect of inlet exhaust and methanol steam on reactor performance was numerically analyzed in detail with computational fluid dynamics. The results showed that the best operating parameters were the counter flow water-to-alcohol (W/A) of 1.3 exhaust inlet velocity of 1.1 m/s and exhaust inlet temperature of 773 K when the inlet velocity and inlet temperature of the reactant were 0.1 m/s and 493 K respectively. At this condition a methanol conversion of 99.4% and thermal efficiency of 28% were achieved together with a hydrogen content of 69.6%.

Developing high-performance electrocatalysts toward hydrogen evolution reaction is important for clean and sustainable hydrogen energy yet still challenging. Herein we report a single-atom strategy to construct excellent metal-organic frameworks (MOFs) hydrogen evolution reaction electrocatalyst (NiRu_0.13-BDC) by introducing atomically dispersed Ru. Significantly the obtained NiRu_0.13-BDC exhibits outstanding hydrogen evolution activity in all pH especially with a low overpotential of 36 mV at a current density of 10 mA cm⁻² in 1 M phosphate buffered saline solution which is comparable to commercial Pt/C. X-ray absorption fine structures and the density functional theory calculations reveal that introducing Ru single-atom can modulate electronic structure of metal center in the MOF leading to the optimization of binding strength for H₂O and H* and the enhancement of HER performance. This work establishes single-atom strategy as an efficient approach to modulate electronic structure of MOFs for catalyst design.

The role of hydrogen in fatigue failure of low strength steels is not as well understood as of high strength steels in very high cycle fatigue regime. In this work axially cyclic tests on a low strength Cr-Ni-Mo-V steel with charged hydrogen were carried out up to the very high cycle fatigue regime under ultrasonic frequency to examine the degradation of fatigue strength and associated failure mechanisms. Results show that the S-N curves show a continuously decreasing mode and hydrogen-charged specimens have lower fatigue strength and shorter fatigue lifetime as compared with as-received specimens. It is concluded that the hydrogen trapped by inclusions drives interior micro-defects as dominant crack initiation site and has a clear link to the initiation and early growth of interior fatigue cracks.

Magnesium hydride (MgH₂) is a potential material for solid-state hydrogen storage. However the thermodynamic and kinetic properties are far from practical application in the current stage. In this work two-dimensional vanadium carbide (V₂C) MXene with layer thickness of 50−100 nm was fist synthesized by selectively HF-etching the Al layers from V₂AlC MAX phase and then introduced into MgH2 to improve the hydrogen sorption performances of MgH2. The onset hydrogen desorption temperature of MgH₂ with V2C addition is significantly reduced from 318 °C for pure MgH2 to 190 °C with a 128 °C reduction of the onset temperature. The MgH₂+ 10 wt% V₂C composite can release 6.4 wt% of H₂ within 10 min at 300 °C and does not loss any capacity for up to 10 cycles. The activation energy for the hydrogen desorption reaction of MgH₂ with V₂C addition was calculated to be 112 kJ mol−1 H₂ by Arrhenius's equation and 87.6 kJ mol−1 H₂ by Kissinger's equation. The hydrogen desorption reaction enthalpy of MgH₂ + 10 wt% V₂C was estimated by van't Hoff equation to be 73.6 kJ mol−1 H₂ which is slightly lower than that of the pure MgH₂ (77.9 kJ mol−1 H₂). Microstructure studies by XPS TEM and SEM showed that V₂C acts as an efficient catalyst for the hydrogen desorption reaction of MgH₂. The first-principles density functional theory (DFT) calculations demonstrated that the bond length of Mg−H can be reduced from 1.71 Å for pure MgH₂ to 2.14 Å for MgH₂ with V₂C addition which contributes to the destabilization of MgH₂. This work provides a method to significantly and simultaneously tailor the hydrogen sorption thermodynamics and kinetics of MgH₂ by two-dimensional MXene materials.

Plastic pre-strains were applied to the metastable 304L austenitic stainless steel at both room temperature (20 °C) and higher temperatures (i.e. 50 80 and 100 °C) and then the hydrogen embrittlement (HE) susceptibility of the steel was evaluated by cathodically hydrogen-charging and tensile testing. The 20 °C pre-strain greatly strengthened the steel but simultaneously significantly increased the HE susceptibility of the steel since α′ martensite was induced by the pre-strain causing the pre-existence of α′ martensite which provided “highways” for hydrogen to transport deep into the steel during the hydrogen-charging. Although the warm pre-strains did not strengthen the steel as significantly as the 20 °C pre-strain they retained the HE resistance of the steel. This is because the higher temperatures particularly 80 and 100 °C suppressed the α′ martensite transformation during the pre-straining. Pre-strain at a temperature slightly higher than room temperature has a potential to strengthen the metastable 304L austenitic stainless steel without compromising its initial HE resistance.

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.

Fuel cells are the most clean and efficient power source for vehicles. In particular proton exchange membrane fuel cells (PEMFCs) are the most promising candidate for automobile applications due to their rapid start-up and low-temperature operation. Through extensive global research efforts in the latest decade the performance of PEMFCs including energy efficiency volumetric and mass power density and low temperature startup ability have achieved significant breakthroughs. In 2014 fuel cell powered vehicles were introduced into the market by several prominent vehicle companies. However the low durability and high cost of PEMFC systems are still the main obstacles for large-scale industrialization of this technology. The key materials and components used in PEMFCs greatly affect their durability and cost. In this review the technical progress of key materials and components for PEMFCs has been summarized and critically discussed including topics such as the membrane catalyst layer gas diffusion layer and bipolar plate. The development of high-durability processing technologies is also introduced. Finally this review is concluded with personal perspectives on the future research directions of this area.

Hydrogen production by electrolysis is considered an essential means of consuming renewable energy in the future. However the current assessment of the potential of renewable energy electrolysis for hydrogen production is relatively simple and the perspective is not comprehensive. Here we established a Combined Wind and Solar Electrolytic Hydrogen system considering the influence of regional wind-solar-load characteristics and transmission costs to evaluate the hydrogen production potential of 31 provincial-level regions in China in 2050. The results show that in 2050 the levelized cost of hydrogen (LCOH) in China’s provincial regions will still be higher than 10 ¥/kg which is not cost-competitive compared to the current hydrogen production from fossil fuels. It is more cost-effective to deploy wind turbines than photovoltaic in areas with similar wind and solar resources or rich in wind resources. Wind-solar differences impact LCOH equipment capacity configuration and transmission cost composition while load fluctuation significantly impacts LCOH and electricity storage configuration. In addition the sensitivity analysis of 11 technical and economic parameters showed differences in the response performance of LCOH changes to different parameters and the electrolyzer conversion efficiency had the most severe impact. The analysis of subsidy policy shows that for most regions (except Chongqing and Xizang) subsidizing the unit investment cost of wind turbines can minimize LCOH. Nevertheless from the perspective of comprehensive subsidy effect subsidy cost and hydrogen energy development it is more cost-effective to take subsidies for electrolysis equipment with the popularization of hydrogen

To address the severity of the wind and light abandonment problem and the economics of hydrogen energy production and operation this paper explores the problem of multi-cycle resource allocation optimization of hydrogen storage systems for coal–wind–solar power generation. In view of the seriousness of the problem of abandoning wind and photovoltaic power and the economy of hydrogen production and operation the node selection and scale setting issues for hydrogen production and storage as well as decision-making problems such as the capacity of new transmission lines and new pipelines and route planning are studied. This research takes the satisfaction of energy supply as the basic constraint and constructs a multi-cycle resource allocation optimization model for an integrated energy system aiming to achieve the maximum benefit of the whole system. Using data from Inner Mongolia where wind abandonment and power limitation are severe and Beijing and Shanxi provinces where hydrogen demand is high this paper analyzes the benefits of the hydrogen storage system for coal–wind–solar power generation and explores the impact of national subsidy policies and technological advances on system economics.

In recent years hydrogen is rapidly developing because it is environmentally friendly and sustainable. In this case hydrogen energy storage systems (HESSs) can be widely used in the distribution network. The application of hybrid electric-hydrogen energy storage systems can solve the adverse effects caused by renewable energy access to the distribution network. In order to ensure the rationality and effectiveness of energy storage systems (ESSs) configuration economic indicators of battery energy storage systems (BESSs) and hydrogen energy storage systems power loss and voltage fluctuation are chosen as the fitness function in this paper. Meanwhile multi-objective particle swarm optimization (MOPSO) is used to solve Pareto non-dominated set of energy storage systems’ optimal configuration scheme in which the technique for order preference by similarity to ideal solution (TOPSIS) based on information entropy weight (IEW) is used select the optimal solution in Pareto non-dominated solution set. Based on the extended IEEE-33 system and IEEE-69 system the rationality of energy storage systems configuration scheme under 20% and 35% renewable energy penetration rate is analyzed. The simulation results show that the power loss can be reduced by 7.9%–22.8% and the voltage fluctuation can be reduced by 40.0%–71% when the renewable energy penetration rate is 20% and 35% respectively in IEEE-33 and 69 nodes systems. Therefore it can be concluded that the locations and capacities of energy storage systems obtained by multi-objective particle swarm optimization can improve the distribution network stability and economy after accessing renewable generation.

A better understanding of chemical kinetics under volumetric expansion is important for a number of situations relevant to industrial safety including detonation diffraction and direct initiation reflected shock-ignition at obstacles ignition behind a decaying shock among others. The ignition of stoichiometric hydrogen-air mixtures was studied using 0D numerical simulations with time-dependent specific volume variations. The competition between chemical energy release and expansion-induced cooling was characterized for different cooling rates and mathematical forms describing the shock decay rate. The critical conditions for reaction quenching were systematically determined and the thermo-chemistry dynamics were analyzed near the critical conditions.