Ústav elektrotechnologie

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Assessing the Carbon Footprint of Viticultural Production in Central European Conditions
(MDPI, 2024-07-31) Bača, Petr; Mašán, Vladimír; Vanýsek, Petr; Burg, Patrik; Binar, Tomáš; Burgová, Jana; Abrham, Zdeněk
A number of factors will increasingly play a role in the sustainability of wine production in the coming period. The current situation suggests that the analysis of energy consumption and greenhouse gas (GHG) emissions will play a particularly important role. The so-called carbon footprint, expressed in CO2 equivalents, is used to express the sum of GHG emissions. This study presents an analysis of vine cultivation in a particular Central European region, with the main focus on quantifying the inputs, yield, fuel consumption, and GHG emissions. The emphasis was placed on conventional, integrated, and ecological production systems of growing, evaluated with the help of the developed AGROTEKIS version 5 software. A total of 30 wine-grower entities in the Morava wine-growing region, the subregion Velk & eacute; Pavlovice, in the Czech Republic weather climate, were included in the input data survey. By analyzing the aggregated values, the real savings in energy and curbing of CO2 emissions of vineyards could be observed, relating to individual work procedures with lower energy demand used in the vineyard treatment as well as the amounts and doses of agrochemicals used. The average values of the total impacts did not show any statistically significant differences between the conventional (971 +/- 78 kg CO2eqha-1year-1) and integrated production systems (930 +/- 62 kg CO2eqha-1year-1), whereas the values for the ecological production system were significantly higher (1479 +/- 40 kg CO2eqha-1year-1). The results show that growing vines under ecological production conditions generates a higher proportion of the carbon footprint than under conventional production conditions. Overall, the best results can be achieved in an integrated production system.
Novel Cu(II)-based metal-organic framework STAM-1 as a sulfur host for Li-S batteries
(NATURE PORTFOLIO, 2024-04-22) Niščáková, V.; Almáši, Miroslav; Capková, Dominika; Kazda, Tomáš; Čech, Ondřej; Čudek, Pavel; Petruš, Ondrej; Volavka, D.; Orinaková, Renáta; Straková Fedorková, Andrea
Due to the increasing demand for energy storage devices, the development of high-energy density batteries is very necessary. Lithium-sulfur (Li-S) batteries have gained wide interest due to their particularly high-energy density. However, even this type of battery still needs to be improved. Novel Cu(II)-based metal-organic framework STAM-1 was synthesized and applied as a composite cathode material as a sulfur host in the lithium-sulfur battery with the aim of regulating the redox kinetics of sulfur cathodes. Prepared STAM-1 was characterized by infrared spectroscopy at ambient temperature and after in-situ heating, elemental analysis, X-ray photoelectron spectroscopy and textural properties by nitrogen and carbon dioxide adsorption at - 196 and 0 degrees C, respectively. Results of the SEM showed that crystals of STAM-1 created a flake-like structure, the surface was uniform and porous enough for electrolyte and sulfur infiltration. Subsequently, STAM-1 was used as a sulfur carrier in the cathode construction of a Li-S battery. The charge/discharge measurements of the novel S/STAM-1/Super P/PVDF cathode demonstrated the initial discharge capacity of 452 mAh g-1 at 0.5 C and after 100 cycles of 430 mAh g-1, with Coulombic efficiency of 97% during the whole cycling procedure at 0.5 C. It was confirmed that novel Cu-based STAM-1 flakes could accelerate the conversion of sulfur species in the cathode material.
Heat Effects during the Operation of Lead-Acid Batteries
(MDPI, 2024-04-27) Bača, Petr; Vanýsek, Petr; Langer, Martin; Zimáková, Jana; Chladil, Ladislav
Thermal events in lead-acid batteries during their operation play an important role; they affect not only the reaction rate of ongoing electrochemical reactions, but also the rate of discharge and self-discharge, length of service life and, in critical cases, can even cause a fatal failure of the battery, known as “thermal runaway.” This contribution discusses the parameters affecting the thermal state of the lead-acid battery. It was found by calculations and measurements that there is a cooling component in the lead-acid battery system which is caused by the endothermic discharge reactions and electrolysis of water during charging, related to entropy change contribution. Thus, under certain circumstances, it is possible to lower the temperature of the lead-acid battery during its discharging. The Joule heat generated on the internal resistance of the cell due to current flow, the exothermic charging reaction, and above all, the gradual increase in polarization as the cell voltage increases during charging all contribute to the heating of the cell, overtaking the cooling effect. Of these three sources of thermal energy, Joule heating in polarization resistance contributes the most to the temperature rise in the lead-acid battery. Thus, the maximum voltage reached determines the slope of the temperature rise in the lead-acid battery cell, and by a suitably chosen limiting voltage, it is possible to limit the danger of the “thermal runaway” effect. The overall thermal conditions of the experimental cell are significantly affected by the ambient temperature of the external environment and the rate of heat transfer through the walls of the calorimeter. A series of experiments with direct temperature measurement of individual locations within a lead-acid battery uses a calorimeter made of expanded polystyrene to minimize external influences. A hitherto unpublished phenomenon is discussed whereby the temperature of the positive electrode was lower than that of the negative electrode throughout the discharge, while during charging, the order was reversed and the temperature of the positive electrode was higher than that of the negative electrode throughout the charge. The authors relate this phenomenon to the higher reaction entropy change of the active mass of the positive electrode than that of the negative electrode.
Carrageenan as an Ecological Alternative of Polyvinylidene Difluoride Binder for Li-S Batteries
(MDPI, 2021-09-26) Kazda, Tomáš; Capková, Dominika; Jaššo, Kamil; Straková Fedorková, Andrea; Shambel, Elena; Markevich, Alex; Sedlaříková, Marie
Lithium-sulfur batteries are one of the most promising battery systems nowadays. However, this system is still not suitable for practical application because of the number of shortcomings that limit its cycle life. One of the main problems related to this system is the volumetric change during cycling. This deficiency can be compensated by using the appropriate binder. In this article, we present the influence of a water-soluble binder carrageenan on the electrochemical properties of the Li-S battery. The electrode with a carrageenan binder provides good stability during cycling and at high C-rates. Electrochemical testing was also carried out with a small prototype pouch cell with a capacity of 16 mAh. This prototype pouch cell with the water-based carrageenan binder showed lower self-discharge and low capacity drop. Capacity decreased by 7% after 70 cycles.
Chemical Delamination Applicable to a Low-Energy Recycling Process of Photovoltaic Modules
(MDPI, 2023-10-26) Vaněk, Jiří; Jandová, Kristýna; Vanýsek, Petr; Maule, Petr
This work follows the current trend and need to ensure the best recyclability of retired materials. This paper focuses on experiments with chemical delamination of polymer layers on crystalline silicon photovoltaic cells. The aim of the study is to separate individual components of a PV module so that the components can be subsequently recycled with low energy demand. The ultimate goal is to separate whole silicon cells for reuse rather than for recycling. Several solvents (e.g., toluene, cyclohexane, tetrahydrofuran, and the commercial solvent U 6002 (a mixture of xylene and 2-ethoxyethylacetate)) were used to disrupt the polymer layers. The results showed toluene to be the most effective solvent, which acted the fastest and was able to disrupt the EVA (ethylene-vinyl acetate) film structure the most. The main problem of the investigated chemical delamination was the concurrent solvent absorption by the EVA film. This phenomenon was observed for all solvents. The absorption prevented the dissolution of the EVA film and changed its dimension, causing the adhering silicon cells to crack. While, as the final experiment shows, chemical delamination is, as done, a more energy-intensive process in terms of total energy consumption than the current chemical mechanical processes, we propose in the next development the recapture of toluene from the swollen EVA.

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