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The accelerator-driven sub-critical system is driven by external neutron sources, which are generated by the spallation reaction and maintain the stable operation of the sub-critical core, while the external neutron source increases the complexity of reactor neutron kinetic processes. This article focuses on simulation analysis of neutron space–time kinetics with a dynamic analysis code, which is developed based on the improved quasi-static approximation and Monte Carlo neutron transport method. The amplitude function and shape functions are solved to achieve the dynamics simulation process. Then, the transient responses of beam interruptions and reactivity insertions are calculated and analyzed for an experimental facility. To further verify the correctness and reliability of dynamic behavior, the simulation results are compared with experimental values, and the results show that the normalized neutron fluxes varying with time are in good agreement with the corresponding values. It can be concluded that the improved quasi-static coupled probability theory method can be used to solve the neutron space–time kinetic problem of the experimental facility, and the results are reliable.

In this study, the hybrid power system of the diesel, as the main power source, and new energy, as the auxiliary energy is developed. An optimal energy management strategy was proposed for the hybrid ship, aiming to minimize consumption of the fuel. The model of the hybrid power system was established in the MATLAB/SIMULINK simulation environment. The optimal energy management strategy was verified by simulation according to the typical drive cycle of ship compared to original energy management strategy. The simulation results show that the proposed optimization can improve fuel economy while the state of charge of the battery is maintained at reasonable range.

Spinel LiNi0.5Mn1.5O4 as one of the high-energy positive electrode materials for next generation Li-ion batteries has attracted significant interest due to its economic and environmental advantages. However, the sensitivity of this type of material upon short to long term ambient storage conditions and the impact on the electrochemical performances remains poorly explored. Nevertheless, this remains an important aspect for practical large-scale synthesis, storage and utilization. Herein, we study and compare the evolution of surface chemistry, bulk crystal structure and elemental content evolution and distribution of LiNi0.5Mn1.5O4 using a variety of characterization techniques including XPS and STEM-EDS-EELS, as well as electrochemical analysis. We show that Mn species dominate the outer surface (0–5 nm), while Ni and Li are preferentially located further away and in the bulk. The studied LiNi0.5Mn1.5O4 material is found to be stable, with minor changes in surface or bulk characteristics detected, even after 12 months of storage under ambient air conditions. The low surface reactivity to air also accounts for the minor changes to the electrochemical performance of the air-exposed LiNi0.5Mn1.5O4, compared to the pristine material. This study provides guidance for the appropriate storage, handling and processing of this high-performance cathode material.

For zero‐defect wave soldering of double‐sided and multilayer printed circuit boards, the copper through‐hole‐plating must be impervious to gas generated in the laminate for the period of a few seconds while the solder is molten. The kinetics of the gas evolution during soldering have been related quantitatively to the integrity of the plated copper. This in turn is related to the quality of the electroless copper (evaluated using the backlighting test), the nature and distribution of the catalyst (evaluated using X‐ray photoelectron spectroscopy) and the methods and effectiveness of the hole‐wall preparation (evaluated using scanning electron microscopy). The relevance of laboratory measurements has been confirmed on a wide range of industrial production plating lines.

Ultrafast laser-annealing technique for the fabrication of large-grain perovskite films and efficient perovskite solar cells at room temperature.

The pyrolysis of waste disposable paper cups (WDPCs) was investigated using a thermogravimetric analyser coupled with a Fourier transform infrared spectrometer. The activation energies of the pyrolysis reactions were obtained by the Flynn–Wall–Ozawa (FWO) and Kissinger–Akahira–Sunose (KAS) methods respectively. The kinetic model was determined by the master plots method. Thermogravimetric results showed that the highest weight loss rate occurred from 345 to 365 °C as the heating rate was increased from 10 to 30 °C min−1, indicating the pyrolysis of cellulosic material in the WDPC. The weight loss between 400 and 500 °C can be attributed to the decomposition of polyethylene. By analysing the FTIR spectra, it was found that the absorbance of all the evolved gaseous products had peaks at 360 °C due to the decomposition of cellulose fibres and the cracking of polyethylene at 485 °C led to the emergence of a second hydrocarbon peak. Ketones were the most abundant condensable organic products and CO2 was the dominating gaseous product, which can also be produced via secondary cracking of the small molecule organics above 400 °C. Kinetic analysis revealed that the average activation energy of the pyrolysis of the WDPC was 153.75 kJ mol−1 from the FWO method and 151.43 kJ mol−1 from the KAS method. The reaction mechanism can be described by the R3 model.

Microbial fuel cells (MFCs) can potentially be utilized for power generation, but their low power density and low energy storage capabilities remain major bottlenecks for their large-scale development. In this research, a simplistic nitrogen-doped hierarchically porous carbon material (HPC-A) was developed through a one-step carbonization and activation process and was successfully hot-pressed on the carbon cloth (CC) substrate. This process fabricates capacitive bioanodes (HPC-A-CC) that can enhance electricity generation and storage in MFCs. The as-prepared HPC-A-CC anode delivered a power density of 2043.6 mW·m-2 and a cumulative total charge (Qm) of 426.4 ± 13.4C·m-2 at each cycle, which was 2.1 and 34.8 times higher than that of the plain CC anode, respectively. This was a result of the hierarchical and interconnected porous structure, improved hydrophilic surface, and increased number of active centers which host the bacteria for enhanced electron transfer. Electrochemical measurements indicated the superior electrochemical activity and capacitive behavior of the HPC-A-CC anode. Furthermore, biofilm analysis revealed that the HPC-A-CC biofilm exhibited higher cell viability and a more uniform spatial distribution. These findings not only demonstrate the potential of HPC-A-CC for power enhancement in MFCs but also provide a feasible solution to the problem of power generation and demand mismatch in MFC applications.

Parabolic trough power plants are currently the most commercially applied systems for CSP power generation. To improve their cost-effectiveness, one focus of industry and research is the development of processes with other heat transfer fluids than the currently used synthetic oil. One option is the utilization of water/steam in the solar field, the so-called direct steam generation (DSG). Several previous studies promoted the economic potential of DSG technology [1–3]. Analyses’ results showed that live steam parameters of up to 500°C and 120 bars are most promising and could lead to a reduction of the levelized electricity cost (LEC) of about 11% [4]. However, all of these studies only considered plants without thermal energy storage (TES). Therefore, a system analysis including integrated TES was performed by Flagsol GmbH and DLR together with Solar Millennium AG, Schott CSP GmbH and Senior Bergho¨fer GmbH, all Germany. Two types of plants are analyzed and compared in detail: a power plant with synthetic oil and a DSG power plant. The design of the synthetic oil plant is very similar to the Spanish Andasol plants [5] and includes a molten salt two-tank storage system. The DSG plant has main steam parameters of 500 °C and 112 bars and uses phase change material (PCM) for the latent and molten salt for the sensible part of the TES system. To enable comparability, both plants share the same gross electric turbine capacity of 100 MWel, the same TES capacity of nine hours of full load equivalent and the same solar multiple of the collector field of about two. This paper describes and compares both plants’ design, performance and investment. Based on these results, the LEC are calculated and the DSG plant’s potential is evaluated. One key finding is that with currently proposed DSG storage costs, the LEC of a DSG plant could be higher than those of a synthetic oil plant. When considering a plant without TES on the other hand, the DSG system could reduce the LEC. This underlines the large influence of TES and the still needed effort in the development of a commercial storage system for DSG.