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The choice of optimal plant species for phytoremediation and organic fertilization plays an important role in stabilizing the functions of soils contaminated with heavy metals. The influence of nickel, cobalt and cadmium on the biomass yield and calorific value of Festuca rubra, heavy metal concentrations in soil and plants and the microbiological, biochemical and physicochemical proprieties of soil were analyzed in a pot experiment. The tolerance index (TI) describing Festuca rubra’s ability to tolerate heavy metals, as well as the translocation (TF), accumulation (AF) and bioaccumulation (BF) factors of heavy metals in Festuca rubra were calculated. The experiment was conducted in two series: In soil fertilized and not fertilized with compost. Nickel and cobalt significantly inhibited the growth and development of Festuca rubra. The experiment demonstrated that this plant species can be grown on soil contaminated with heavy metals. Festuca rubra contained on average 46.05% C, 34.59% O, 5.91% H, 3.49% N, 0.19% S and 9.76% ash. Festuca rubra has a stable calorific value which is not affected by heavy metals; therefore, biomass harvested from heavy metal-polluted soil can be used for energy generation. The calorific value of Festuca rubra ranged from 15.924 to 16.790 MJ kg−1 plant d.m., and the heat of combustion from 17.696 to 18.576 MJ kg−1. It has a stable calorific value which is not affected by heavy metals, therefore biomass harvested from heavy metal-polluted soil can be used for energy generation. Festuca rubra is particularly useful for the phytostabilization of soil contaminated with cadmium and cobalt. Compost minimizes the adverse effects of heavy metal pollution on the microbiological, biochemical and physicochemical properties of soil.

While silicon anodes hold promise for use in lithium-ion batteries owing to their very high theoretical storage capacity and relatively low discharge potential, they possess a major problem related to their large volume expansion that occurs with battery aging. The resulting stress and strain can lead to mechanical separation of the anode from the current collector and an unstable solid electrolyte interphase (SEI), resulting in capacity fade. Since capacity loss is in part dependent on the cell materials, two different electrodes, Lithium Nickel Oxide or LiNi0.8Co0.15Al0.05O2 (NCA) and LiNi1/3Mn1/3Co1/3O2 (NMC 111), were used in combination with silicon to study capacity fade effects using simulations in COMSOL version 5.5. The results of these studies provide insight into the effects of anode particle size and electrolyte volume fraction on the behavior of silicon anode-based batteries with different positive electrodes. It was observed that the performance of a porous matrix of solid active particles of silicon anode could be improved when the active particles were 150 nm or smaller. The range of optimized values of volume fraction of the electrolyte in the silicon anode were determined to be between 0.55 and 0.40. The silicon anode behaved differently in terms of cell time with NCA and NMC. However, NMC111 gave a high relative capacity in comparison to NCA and proved to be a better working electrode for the proposed silicon anode structure.

The poor operational stability of electrolytes is a persistent impediment in building redox flow battery technology; choosing suitable stability additives is usually the research direction to solve this problem. The effects of five phosphate containing additives (including 1-hydroxyethylidene-1,1-diphosphonic acid (HEDP), hexamethylene diamine tetramethylene phosphonic acid (HDTMPA), amino trimethylene phosphonic acid (ATMPA), sodium ethylenediamine tetramethylene phosphonate (EDTMPS), and diethyl triamine pentamethylene phosphonic acid (DTPMP)) on the thermal stability and electrochemical performance of the positive electrolyte of vanadium redox flow battery were investigated. With 0.5 wt% addition, most of the selected additives were able to improve the thermal stability of the electrolyte. HEDP and HDTMPA extended the stability time of the pentavalent vanadium electrolyte at 50 °C from 5 days (blank sample) to 30 days and 15 days, respectively. The electrochemical performance of the electrolyte was further investigated by cyclic voltammetry, steady state polarization, and electrochemical impedance spectroscopy tests. It was found that most of the additives enhanced the electrochemical activity of the positive electrolyte, and the diffusion coefficients, exchange current densities, and reaction rate constants of V(IV) species became larger with the addition of these additives. It is verified that the thermal stability and electrochemical stability of the electrolyte are significantly improved by the combination of ATMPA + HEDP or ATMPA + HDTMPA. This study provides a new approach to improve the stability of the positive electrolyte for vanadium redox flow battery.

The need for energy-storing technologies with lower environmental impact than Li-ion batteries but similar power metrics has revived research in Zn-based battery chemistries. The application of bio-based materials as a replacement for current components can additionally contribute to an improved sustainability of Zn battery systems. For that reason, bacterial cellulose (BC) was investigated as separator material in Ni-Zn batteries. Following the biotechnological production of BC, the biopolymer was purified, and differently shaped separators were generated while surveying the alterations of its crystalline structure via X-ray diffraction measurements during the whole manufacturing process. A decrease in crystallinity and a partial change of the BC crystal allomorph type Iα to II was determined upon soaking in electrolyte. Electrolyte uptake was found to be accompanied by dimensional shrinkage and swelling, which was associated with partial decrystallization and hydration of the amorphous content. The separator selectivity for hydroxide and zincate ions was higher for BC-based separators compared to commercial glass-fiber (GF) or polyolefin separators as estimated from the obtained diffusion coefficients. Electrochemical cycling showed good C-rate capability of cells based on BC and GF separators, whereas cell aging was pronounced in both cases due to Zn migration and anode passivation. Lower electrolyte retention was concluded as major reason for faster capacity fading due to zincate supersaturation within the BC separator. However, combining a dense BC separator with low zincate permeability with a porous one as electrolyte reservoir reduced ZnO accumulation within the separator and improved cycling stability, hence showing potentials for separator adjustment.

Stress-dominated coal and gas outburst disaster has become one of the main safety problems in deep coal mines. Acoustic emission (AE) or microseismic technology has been viewed as a promising method that can effectively reflect the stress and stability status of rock mass. The AE activity precursor of coal failure is the theoretical basis of this technology. In this study, AE experiments in failure process of coal specimens with different properties and under different stress conditions were performed in laboratory to explore influence factors and their effect of AE activity, and AE activity pattern classification was proposed based on the failure type of coal. The results indicate that the AE activity of different coals under loading are associated with the failure phase, and the evolution pattern of AE activity depends on the failure type of stressed coal. Both the mechanical property and the external stress condition have an important influential effect on the failure type and AE activity pattern in coal failure process. The internal mechanical property decides the inherent tendency of stressed coals to perform brittle or ductile behavior, and the responded AE activity pattern. The contrast of fissure distribution of specimens suggested that fissure structure in coal significantly affects the fracturing mode of coal in uniaxial compression and the AE activity pattern. The external stress condition has a transition effect on AE event energy distribution and AE activity pattern. Under the effect of external stress condition, the energy distribution of AE events was transforming between relative disperse and relative concentration, the failure type and AE activity evolution pattern of coal could appear the brittle-ductile transition. Based on the view of failure type, the pattern of AE activity of coal failure can be classified into three types, i.e., ductile, brittle, and semi-brittle pattern. It is suggested that the high-level AE activity can be viewed as the precursor of brittle instability of coal, and relative quiet phenomenon of AE activity as the precursor of ductile or semi-brittle instability. The research achievement can provide a theoretical base for the prewarning criteria establishment of coal and rock dynamic disasters at depth and improve the insight of AE activity in the coal failure process.

To improve the safety of lithium ion batteries, a multi-component (MC) additive (consisting of vinylene carbonate (VC), 1,3-propylene sulfite (PS) and dimethylacetamide (DMAC)) is used in the baseline electrolyte (1.0 M LiPF6/ethylene carbonate (EC) + diethyl carbonate (DEC)). The electrolyte with the MC additive is named safety electrolyte. The thermal stabilities of fully charged Li(Ni1/3Co1/3Mn1/3)O2 (NCM) mixed with the baseline electrolyte and safety electrolyte, respectively, are investigated using a C80 micro-calorimeter. The electrochemical performances of the NCM/baseline electrolyte/Li and NCM/safety electrolyte/Li half cells are evaluated using galvanostatic charge/discharge, cyclic voltammetry and alternating current (AC) impedance. The experimental results demonstrate that the fully charged NCM-safety electrolyte system releases less heat and reduces the main sharp exothermic peak value to a great extent, with a reduction of 40.6%. Moreover, the electrochemical performances of NCM/safety electrolyte/Li half cells are not worse, and are almost as good as that of the NCM/baseline electrolyte/Li half cells.

Energy storage in an uninterruptible power supply (UPS) is one of the most frequent applications of batteries. This can be found in hospitals, communication centers, public centers, ships, trains, etc. Most frequent industrial methods for battery state-of health estimation require a technician to move to the battery’s location and, in some cases, require the use of heavy equipment and disconnection of the battery from the UPS. For example, in railway applications, trains must stop at the maintenance depot producing significant total costs. This article proposes a new method to assess a battery’s health by measuring the battery’s internal resistance, based on the measurement of its voltage ripple in response to the current ripple imposed by the charger which in most UPS applications is permanently connected to the battery. Unlike most traditional methods, this system makes it possible a continuous on-line and on-board monitoring, and, therefore, it eases condition-based maintenance (CBM). To verify its viability, a low cost measuring prototype has been built and measurements in a railway battery with its charger have been carried out.

The paper presents the results of an investigation into thin single- and triple-layer ZrO2-Sc2O3-based electrolytes prepared using the tape-casting technique in combination with promising electrodes based on La2NiO4+δ and Ni-Ce0.8Sm0.2O2-δ materials. It is shown that pressing and joint sintering of single electrolyte layers allows multilayer structures to be obtained that are free of defects at the layer interface. Electrical conductivity measurements of a triple-layer electrolyte carried out in longitudinal and transverse directions with both direct and alternating current showed resistance of the interface between the layers on the total resistance of the electrolyte to be minimal. Long-term tests have shown that the greatest degradation in resistance over time occurs in the case of an electrolyte with a tetragonal structure. Symmetrical electrochemical cells with electrodes fabricated using a screen-printing method were examined by means of electrochemical impedance spectroscopy. The polarization resistance of the electrodes was 0.45 and 0.16 Ohm∙cm2 at 800 °C for the fuel and oxygen electrodes, respectively. The distribution of relaxation times method was applied for impedance data analysis. During tests of a single solid oxide fuel cell comprising a supporting triple-layer electrolyte having a thickness of 300 microns, a power density of about 160 mW/cm2 at 850 °C was obtained using wet hydrogen as fuel and air as an oxidizing gas.