China, People’s Republic

Excessive consumption of fossil fuels has led to depletion of reserves and environmental crises. Therefore turning to clean energy sources is essential. However these energy sources are intermittent in nature and have problems meeting long-term energy demand. The option suggested by the researchers is to use hybrid energy systems. The aim of this paper is provide the conceptual configuration of a novel energy cycle based on clean energy resources. The novel energy cycle is composed of a wind turbine solar photovoltaic field (PV) an alkaline fuel cell (AFC) a Stirling engine and an electrolyzer. Solar PV and wind turbine convert solar light energy and wind kinetic energy into electricity respectively. Then the generated electricity is fed to water electrolyzer. The electrolyzer decomposes water into oxygen and hydrogen gases by receiving electrical power. So the fuel cell inlets are provided. Next the AFC converts the chemical energy contained in hydrogen into electricity during electrochemical reactions with by-product (heat). The purpose of the introduced cycle is to generate electricity and hydrogen fuel. The relationships defined for the components of the proposed cycle are novel and is examined for the first time. Results showed that the output of the introduced cycle is 10.5 kW of electricity and its electrical efficiency is 56.9%. In addition the electrolyzer uses 9.9 kW of electricity to produce 221.3 grams per hour of hydrogen fuel. The share of the Stirling engine in the output power of the cycle is 9.85% (1033.7 W) which is obtained from the dissipated heat of the fuel cell. In addition wind turbine is capable of generating an average of 4.1 kW of electricity. However 238.6 kW of cycle exergy is destroyed. Two different scenarios are presented for solar field design.

In some areas the problem of wind and solar power curtailment is prominent. Hydrogen energy has the advantage of high storage density and a long storage time. Multi-energy hybrid systems including renewable energies batteries and hydrogen are designed to solve this problem. In order to reduce the power loss of the converter an AC-DC hybrid bus is proposed. A multi-energy experiment platform is established including a wind turbine photovoltaic panels a battery an electrolyzer a hydrogen storage tank a fuel cell and a load. The working characteristics of each subsystem are tested and analyzed. The multi-energy operation strategy is based on state monitoring and designed to enhance hydrogen utilization energy efficiency and reliability of the system. The hydrogen production is guaranteed preferentially and the load is reliably supplied. The system states are monitored such as the state of charge (SOC) and the hydrogen storage level. The rated and ramp powers of the battery and fuel cell and the pressure limit of the hydrogen storage tank are set as safety constraints. Eight different operation scenarios comprehensively evaluate the system’s performance and via physical experiments the proposed operation strategy of the multi-energy system is verified as effective and stable.

Combined cycle biomass calcium looping gasification is proposed for a hydrogen and electricity production (CLGCC–H) system. The process simulation Aspen Plus is used to conduct techno-economic analysis of the CLGCC–H system. The appropriate detailed models are set up for the proposed system. Furthermore a dual fluidized bed is optimized for hydrogen production at 700 °C and 12 bar. For comparison calcium looping gasification with the combined cycle for electricity (CLGCC) is selected with the same parameters. The system exergy and energy efficiency of CLGCC–H reached as high as 60.79% and 64.75% while the CLGCC system had 51.22% and 54.19%. The IRR and payback period of the CLGCC–H system based on economic data are calculated as 17.43% and 7.35 years respectively. However the CLGCC system has an IRR of 11.45% and a payback period of 9.99 years respectively. The results show that the calcium looping gasification-based hydrogen and electricity coproduction system has a promising market prospect in the near future.

Liquid hydrogen is the main fuel of large-scale low-temperature heavy-duty rockets and has become the key direction of energy development in China in recent years. As an important application carrier in the large-scale storage and transportation of liquid hydrogen liquid hydrogen cryogenic storage and transportation containers are the key equipment related to the national defense security of China’s aerospace and energy fields. Due to the low temperature of liquid hydrogen (20 K) special requirements have been put forward for the selection of materials for storage and transportation containers including the adaptability of materials in a liquid hydrogen environment hydrogen embrittlement characteristics mechanical properties and thermophysical properties of liquid hydrogen temperature which can all affect the safe and reliable design of storage and transportation containers. Therefore it is of great practical significance to systematically master the types and properties of cryogenic materials for the development of liquid hydrogen storage and transportation containers. With the wide application of liquid hydrogen in different occasions the requirements for storage and transportation container materials are not the same. In this paper the types and applications of cryogenic materials commonly used in liquid hydrogen storage and transportation containers are reviewed. The effects of low-temperature on the mechanical properties of different materials are introduced. The research progress of cryogenic materials and low-temperature performance data of materials is introduced. The shortcomings in the research and application of cryogenic materials for liquid hydrogen storage and transportation containers are summarized to provide guidance for the future development of container materials. Among them stainless steel is the most widely used cryogenic material for liquid hydrogen storage and transportation vessel but different grades of stainless steel also have different applications which usually need to be comprehensively considered in combination with its low temperature performance corrosion resistance welding performance and other aspects. However with the increasing demand for space liquid hydrogen storage and transportation the research on high specific strength cryogenic materials such as aluminum alloy titanium alloy or composite materials is also developing. Aluminum alloy liquid hydrogen storage and transportation containers are widely used in the space field while composite materials have significant advantages in being lightweight. Hydrogen permeation is the key bottleneck of composite storage and transportation containers. At present there are still many technical problems that have not been solved.

A new MgH₂–PrF₃–Al–Ni composite was prepared by ball milling under hydrogen atmosphere. After initial dehydrogenation and rehydrogenation Pr₃Al₁₁ MgF₂ PrH₃ and Mg₂NiH₄ nanoparticles formed accompanying the main phase MgH₂. The hydrogen absorption-desorption properties were measured by using a Sieverts-type apparatus. The results showed that the MgH₂–PrF₃–Al–Ni composite improved cycle stability and enhanced hydrogen desorption kinetics. The improvement of hydrogen absorption-desorption properties is ascribed to the synergetic effect of the in situ formed Pr₃Al11 MgF₂ PrH₃ and Mg₂NiH₄ nanoparticles. This work provides an important inspiration for the improvement of hydrogen storage properties in Mg-based materials.

Electrical energy storage (EES) such as lithium-ion (Li-ion) batteries can reduce curtailment of renewables maximizing renewable utilization by storing surplus electricity. Several techno-economic analyses have been performed on EES but few have investigated the financial performance. This paper presents a state-of-the-art financial model obtaining novel and significative financial and economics results when applied to Li-ion EES. This work is a significant step forward since traditional analysis on EES are based on oversimplified and unrealistic economic models. A discounted cash flow model for the Li-ion EES is introduced and applied to examine the financial performance of three EES operating scenarios. Real-life solar irradiance load and retail electricity price data from Kenya are used to develop a set of case studies. The EES is coupled with photovoltaics and an anaerobic digestion biogas power plant. The results show the impact of capital cost: the Li-ion project is unprofitable in Kenya with a capital cost of 1500 $/kWh but is profitable at 200 $/kWh. The study shows that the EES will generate a higher profit if it is cycled more frequently (hence a higher lifetime electricity output) although the lifetime is reduced due to degradation.

It has been well known that doping nano-scale catalysts can significantly improve both the kinetics and reversible hydrogen storage capacity of MgH2. However so far it is still a challenge to directly synthesize ultrafine catalysts (e.g. < 5 nm) mainly because of the complicated chemical reaction processes. Here a facile one-step high-energy ball milling process is developed to in situ form ultrafine Ni nanoparticles from the nickel acetylacetonate precursor in the MgH2 matrix. With the combined action of ultrafine metallic Ni and expanded graphite (EG) the formed MgH2–Ni-EG nanocomposite with the optimized doping amounts of Ni and EG can still release 7.03 wt.% H2 within 8.5 min at 300 °C after 10 cycles. At a temperature close to room temperature (50 °C) it can also absorb 2.42 wt.% H2 within 1 h It can be confirmed from the microstructural characterization analysis that the in situ formed ultrafine metallic Ni is transformed into Mg2Ni/Mg2NiH4 in the subsequent hydrogen absorption and desorption cycles. It is calculated that the dehydrogenation activation energy of the MgH2–Ni-EG nanocomposite is also reduced obviously in comparison with the pure MgH2. Our work provides a methodology to significantly improve the hydrogen storage performance of MgH2 by combining the in situ formed and uniformly dispersed ultrafine metallic catalyst from the precursor and EG.

To address the challenge of highly efficient water splitting into H₂ successful fabrication of novel porous three-dimensional Ni-doped CoP₃ nanowall arrays on carbon cloth was realized resulting in an effective self-supported electrode for the electrocatalytic hydrogen-evolution reaction. The synthesized samples exhibit rough curly and porous structures which are beneficial for gaseous transfer and diffusion during the electrocatalytic process. As expected the obtained Ni-doped CoP₃ nanowall arrays with a doping concentration of 7% exhibit the promoted electrocatalytic activity. The achieved overpotentials of 176 mV for the hydrogen-evolution reaction afford a current density of 100 mA cm⁻² which indicates that electrocatalytic performance can be dramatically enhanced via Ni doping. The Ni-doped CoP₃ electrocatalysts with increasing catalytic activity should have significant potential in the field of water splitting into H₂. This study also opens an avenue for further enhancement of electrocatalytic performance through tuning of electronic structure and d-band center by doping.

A study was carried out on the valorization of different waste plastics (HDPE PP PS and PE) their mixtures and biomass/HDPE mixtures by means of pyrolysis and in line oxidative steam reforming. A thermodynamic equilibrium simulation was used for determining steam reforming data whereas previous experimental results were considered for setting the pyrolysis volatile stream composition. The adequacy of this simulation tool was validated using experimental results obtained in the pyrolysis and in line steam reforming of different plastics. The effect the most relevant process conditions i.e. temperature steam/plastic ratio and equivalence ratio have on H2 production and reaction enthalpy was evaluated. Moreover the most suitable conditions for the oxidative steam reforming of plastics of different nature and their mixtures were determined. The results obtained are evidence of the potential interest of this novel valorization route as H2 productions of up to 25 wt% were obtained operating under autothermal conditions.

Hydrogen-microvoid interactions were studied via unit cell analyses with different hydrogen concentrations. The absolute failure strain decreases with hydrogen concentration but the failure loci were found to follow the same trend dependent only on stress triaxiality in other words the effects of geometric constraint and hydrogen on failure are decoupled. Guided by the decoupling principle a hydrogen informed Gurson model is proposed. This model is the first practical hydrogen embrittlement simulation tool based on the hydrogen enhanced localized plasticity (HELP) mechanism. It introduces only one additional hydrogen related parameter into the Gurson model and is able to capture hydrogen enhanced internal necking failure of microvoids with accuracy; its parameter calibration procedure is straightforward and cost efficient for engineering purpose