China, People’s Republic

Compact-tension (CT) specimens made of low alloy 30CrMo steels were hydrogen-charged and then subjected to the fracture toughness test. The experimental results revealed that the higher crack propagation and the lower crack growth resistance (CTOD-R curve) are significantly noticeable with increasing hydrogen embrittlement (HE) indexes. Moreover the transition in the microstructural fracture mechanism from ductile (microvoid coalescence (MVC)) without hydrogen to a mixed quasi-cleavage (QC) fracture and QC + intergranular (IG) fracture with hydrogen was observed. The hydrogen-enhanced decohesion (HEDE) mechanism was characterized as the dominant HE mechanism. According to the experimental testing the coupled problem of stress field and hydrogen diffusion field with cohesive zone stress analysis was employed to simulate hydrogen-assisted brittle fracture behavior by using ABAQUS software. The trapezoidal traction-separation law (TSL) was adopted and the initial TSL parameters from the best fit to the load-displacement and J-integral experimental curves without hydrogen were calibrated for the critical separation of 0.0393 mm and the cohesive strength of 2100 MPa. The HEDE was implemented through hydrogen influence in the TSL and to estimate the initial hydrogen concentration based on matching numerical and experimental load-line displacement curves with hydrogen. The simulation results show that the general trend of the computational CTOD-R curves corresponding to initial hydrogen concentration is almost the same as that obtained from the experimental data but in full agreement the computational CTOD values being slightly higher. Comparative analysis of numerical and experimental results shows that the coupled model can provide design and prediction to calculate hydrogen-assisted fracture behavior prior to extensive laboratory testing provided that the material properties and properly calibrated TSL parameters are known.

Due to the low efficiency and high pollution of conventional internal combustion engine vehicles the fuel cell hybrid electric vehicles are expected to play a key role in the future of clean energy transportation attributed to the long driving range short hydrogen refueling time and environmental advantages. The development of energy management strategies has an important impact on the economy and durability but most strategies ignore the aging of fuel cells and the corresponding impact on hydrogen consumption. In this paper a rule-based fuzzy control strategy is proposed based on the constructed data-driven online estimation model of fuel cell health. Then a genetic algorithm is used to optimize this fuzzy controller where the objective function is designed to consider both the economy and durability by combining the hydrogen consumption cost and the degradation cost characterized by the fuel cell health status. Considering that the rule-based strategy is more sensitive to operating conditions this paper uses an artificial neural network for predictive control. The results are compared with those obtained from the genetic algorithm optimized fuzzy controller and are found to be very similar where the prediction accuracy is assessed using MAPE RMSE and 10-fold cross-validation. Experiments show that the developed strategy has a good generalization capability for variable driving cycles.

Hydrogen is an ideal clean energy source that can be used as an energy storage medium for renewable energy sources. The water electrolysis hydrogen production technology which is one of the mainstream hydrogen production methods can be used to produce high-purity hydrogen and other energy sources can be converted into hydrogen storage by electrolysis. Hydrogen production by alkaline water electrolysis and hydrogen production by PEM electrolysis are all water electrolysis hydrogen production technologies that have been industrially applied. From the application point of view the paper compares the working principle of the two kinds of electrolyzers the process flow of hydrogen production equipment advantages and disadvantages. This article provides a reference for relevant researchers.

Presently hydrogen is for ~50% produced by steam reforming of natural gas – a process leading to significant emissions of greenhouse gas (GHG). About 30% is produced from oil/naphtha reforming and from refinery/chemical industry off-gases. The remaining capacity is covered for 18% from coal gasification 3.9% from water electrolysis and 0.1% from other sources. In the foreseen future hydrogen economy green hydrogen production methods will need to supply hydrogen to be used directly as fuel or to generate synthetic fuels to produce ammonia and other fertilizers (viz. urea) to upgrade heavy oils (like oil sands) and to produce other chemicals. There are several ways to produce H2 each with limitations and potential such as steam reforming electrolysis thermal and thermo-chemical water splitting dark and photonic fermentation; gasification and catalytic decomposition of methanol. The paper reviews the fundamentals and potential of these alternative process routes. Both thermo-chemical water splitting and fermentation are marked as having a long term but high "green" potential.

Hydrogen as an energy carrier is very versatile in energy storage applications. Developments in novel sustainable technologies towards a CO2-free society are needed and the exploration of all-solid-state batteries (ASSBs) as well as solid-state hydrogen storage applications based on metal hydrides can provide solutions for such technologies. However there are still many technical challenges for both hydrogen storage material and ASSBs related to designing low-cost materials with low-environmental impact. The current materials considered for all-solid-state batteries should have high conductivities for Na+ Mg2+ and Ca2+ while Al3+-based compounds are often marginalised due to the lack of suitable electrode and electrolyte materials. In hydrogen storage materials the sluggish kinetic behaviour of solid-state hydride materials is one of the key constraints that limit their practical uses. Therefore it is necessary to overcome the kinetic issues of hydride materials before discussing and considering them on the system level. This review summarizes the achievements of the Marie Skłodowska-Curie Actions (MSCA) innovative training network (ITN) ECOSTORE the aim of which was the investigation of different aspects of (complex) metal hydride materials. Advances in battery and hydrogen storage materials for the efficient and compact storage of renewable energy production are discussed.

Hydrogen energy vehicles are being increasingly widely used. To ensure the safety of hydrogenation stations research into the detection of hydrogen leaks is required. Offline analysis using data machine learning is achieved using Spark SQL and Spark MLlib technology. In this study to determine the safety status of a hydrogen refueling station we used multiple algorithm models to perform calculation and analysis: a multi-source data association prediction algorithm a random gradient descent algorithm a deep neural network optimization algorithm and other algorithm models. We successfully analyzed the data including the potential relationships internal relationships and operation laws between the data to detect the safety statuses of hydrogen refueling stations.

Operating chemical looping process at mid-temperatures (550-750 oC) presents exciting potential for the stable production of hydrogen. However the reactivity of oxygen carriers is compromised by the detrimental effect of the relatively low temperatures on the redox kinetics. Although the reactivity at mid-temperature can be improved by the addition of noble metals the high cost of these noble metal containing materials significantly hindered their scalable application. In the current work we propose to incorporate earth-abundant metals into the iron-based spinel for hydrogen production in a chemical looping scheme at mid-temperatures. Mn0.2Co0.4Fe2.4O4 shows a high hydrogen production rate at the average rate of ∼0.62 mmol.g-1.min-1 and a hydrogen yield of ∼9.29 mmol.g-1 with satisfactory stability over 20 cycles at 550 oC. The mechanism studies manifest that the enhanced hydrogen production performance is a result of the improved oxygen-ion conductivity to enhance reduction reaction and high reactivity of reduced samples with steam. The performance of the oxygen carriers in this work is comparable to those noble-metal containing materials enabling their potential for industrial applications.

To improve the utilization rate of the energy industry and reduce high energy consumption and pollution caused by coal chemical industries in north western China a planning scheme of a wind‐coal coupling energy system was developed. This scheme involved the analysis method evaluation criteria planning method and optimization operation check for the integration of a comprehensive evaluation framework. A system was established to plan the total cycle revenue to maximize the net present value of the goal programming model and overcome challenges associated with the development of new forms of energy. Subsequently the proposed scheme is demonstrated using a 500‐MW wind farm. The annual capacity of a coal‐to‐methanol system is 50000. Results show that the reliability of the wind farm capacity and the investment subject are the main factors affecting the feasibility of the wind‐coal coupled system. Wind power hydrogen production generates O2 and H2 which are used for methanol preparation and electricity production in coal chemical systems respectively. Considering electricity price constraints and environmental benefits a methanol production plant can construct its own wind farm matching its output to facilitate a more economical wind‐coal coupled system. Owing to the high investment cost of wind power plants an incentive mechanism for saving energy and reducing emissions should be provided for the wind‐ coal coupled system to ensure economic feasibility and promote clean energy transformation.

In this study hydrogen-storage glass microballoons were introduced into emulsion explosives to improve the detonation performance of the explosives. The effect of hydrogen-storage pressure on the detonation characteristics of emulsion explosives was systematically investigated. Detonation velocity experiments shows that the change of sensitizing gas and the increase of hydrogen pressure have different effects on the detonation velocity. The experimental parameters of underwater explosion increase first and then decreases with the increase of hydrogen pressure. The decrease of these parameters indicates that the strength of glass microballoons is the limiting factor to improve the detonation performance of hydrogen-storage emulsion explosives. Compared with the traditional emulsion explosives the maximum peak pressure of shock wave of hydrogen-storage emulsion explosives increases by 10.6% at 1.0 m and 10.2% at 1.2 m the maximum values of shock impulse increase by 5.7% at 1.0 m and 19.4% at 1.2 m. The stored hydrogen has dual effects of sensitizers and energetic additives which can improve the energy output of emulsion explosives.

As a promising hydrogen storage material the practical application of magnesium is obstructed by the stable thermodynamics and sluggish kinetics. In this paper three kinds of NiTiO₃ catalysts with different mole ratio of Ni to Ti were successfully synthesized and doped into nanocrystalline Mg to improve its hydrogen storage properties. Experimental results indicated that all the Mg-NiTiO₃ composites showed prominent hydrogen storage performance. Especially the Mg-NiTiO3/TiO₂ composite could take up hydrogen at room temperature and the apparent activation energy for hydrogen absorption was dramatically decreased from 69.8 ± 1.2 (nanocrystalline Mg) kJ/mol to 34.2 ± 0.2 kJ/mol. In addition the hydrogenated sample began to release hydrogen at about 193.2 °C and eventually desorbed 6.6 wt% H₂. The desorption enthalpy of the hydrogenated Mg-NiTiO₃ -C was estimated to be 78.6 ± 0.8 kJ/mol 5.3 kJ/mol lower compared to 83.9 ± 0.7 kJ/mol of nanocrystalline Mg. Besides the sample revealed splendid cyclic stability during 20 cycles. No obvious recession occurred in the absorption and desorption kinetics and only 0.3 wt% hydrogen capacity degradation was observed. Further structural analysis demonstrates that nanosizing and catalyst doping led to a synergistic effect on the enhanced hydrogen storage performance of Mg-NiTiO₃ -C composite which might serve as a reference for future design of highly effective hydrogen storage materials.