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The aim of the paper is to examine the performance of molten carbonate fuel cell, which is supplied with a raw bioethanol, i.e. bioethanol which origins directly from fruit fermentation, without pre-treatment of fermentation products. The composition of raw bioethanol was precisely determined and then the impact of raw bioethanol on the degradation of molten carbonate fuel cells was examined. Steam to carbon ratio of the biofuel has been determined as 5.7 (in comparison to stoichiometry of reaction) which allowed for estimation of hydrogen production during steam reforming process taking place in the anode channel. The results in the form of current-voltage curve was obtained and compared with the same fuel cell fed with pure hydrogen, while the amount of hydrogen was defined as identical with the one after steam reforming of biofuel taking place in the nickel anode channel. Relevant literature studies were focused on the purified fuel or examination of the impact of individual components. Our study proved carbon deposition is not a problem, however solid particles contamination in fermentation product makes it impossible to use fuel cell fueled with fermentation product for longer periods, and prior to supplying fuel cell the bioethanol purification is required. A raw biofuel with its impurities did not have any impact on the anode and current collector surface from physical point of view, but Electrochemical Impedance Spectroscopy analysis shows visible increase of ohmic loses. • Homemade first generation bioethanol composition have been examined. • Manufactured bioethanol has been delivered directly to the MCFC anode without purification. • Performance of MCFC fueled with impure bioethanol has been investigated. • Effect of steam reforming for hydrogen generation and steam to carbon ratio were evaluated. • Pollution on the anode after cell operation was investigated with SEM and EIS. [ABSTRACT FROM AUTHOR]

In order to improve the energy efficiency of the Sabatier reactor-based power-to-gas process, molten carbonate fuel cells and solid oxide electrolyzers were installed instead of a conventional amine CO 2 capture system and a classical alkaline electrolyzer. The plant is a multi-module prototype with a nominal capacity of 50 kW consisting of two SOE-MCFC units. The system was commissioned in 2022. The article describes the theoretical basis. The initial assumptions that were formulated at the stage of preparing for the research investment, as well as the deviations from them that became the result of detailed design were presented. The developed startup and shutdown procedures, as well as the first results of pioneering research were shown. The trial operation of the system was intended to provide information on integrated SOE-MCFC module and its performance and efficiency. The basic barriers for market implementation and recommendations for future research were discussed. The optimal operating point for hydrogen production needed 35.8 kWh/kgH 2. Thus, electrical energy conversion to chemical energy efficiency is 93.9%. Flow preheating and electrical auxiliary heater power are not included. An MCFC at its ideal functioning point (around 4 kW el) outputs 5.4 kg/h of CO 2 separated. • Operational experience of upgraded novel P2G installation is reported. • A start-up procedure of MCFC-SOE tandem in proposed and experimentally verified. • Energy required for synthesis of a kilogram of hydrogen was 35.8 kWh/kgH 2. [ABSTRACT FROM AUTHOR]

This paper presents research on the impact of the material microstructure on the performance of Molten Carbonate Fuel Cells (MCFC). The study is motivated by the need to increase the operation time of MCFC stacks. As the MCFC stacks are mainly composed of porous materials, the paper shows the impact of the porosity on both fuel cell performance and degradation rate. The study is based on the mathematical model, validated through experiments with varying microstructure parameters, achieving an overall relative error of 8%. The study evaluated the performance of MCFC using anodes with different porosity and found that increasing anode porosity from 40% to 70% led to a nearly two-fold increase in maximum power density. However, from both the degradation test and polarization curves, the optimal level of porosity for the anode is around 55%. The porosity level at 55% ensures the highest catalytic surface of the electrodes and is a compromise between the mechanical properties of the electrode and its electrochemical properties. • New approach of 0D model of MCFC including materials microstructure influence is proposed. • The new model is prepared in MS Excel and Aspen HYSYS environments. • Experimental investigation for materials with predefined microstructire parameters was performed for model validation. • Variant analysis is presented for different porosity, tortuosity and constrictivity of MCFC anode. • An optimal scenario is suggested based on modleing results. [ABSTRACT FROM AUTHOR]

[Display omitted] • Electrolyzer and fuel cell integrated in an enhanced power-to-gas system. • No energy penalty for CO 2 capture, in a system with lower power requirements. • CO 2 separation exceeds 90 percent. This study outlines a concept for improving a power-to-gas (P2G) system through the implementation of highly efficient high-temperature electrolysis combined with a molten carbonate fuel cell (MCFC) as a CO 2 capture unit for a power plant. Laboratory scale experiments demonstrate that the MCFC could be used for CO 2 separation, opening the way to capture of CO 2 from flue gases at coal-fired power stations, while maintaining both high electric efficiency and a high CO 2 separation factor. Improved energy efficiency can be achieved by the lower electricity requirement of high temperature electrolysis compared to other technologies. Results obtained from experimental investigations show that a CO 2 separation rate in excess of 90 % is achievable through adjusting the cathode inlet flow. It should be noted that flue gas must be mixed with air before delivery to the MCFC. Controlled flow of inlet gases to the anode can raise electric efficiency to above 35 % for both laboratory-size and full-scale MCFC. The benefits of the concept are manifested by lower power consumption of the system and no energy penalty for the CO 2 capture process. Additionally, the system enjoys good thermal management because all devices run at elevated temperatures (Sabatier reactor at 300 °C, MCFC at 650 °C, solid oxide electrolyzer at 700–800 °C). The proposed improvements increase the system's competitiveness relative to alternative P2G systems and reduce the price of substitute natural gas. Secondly, it will eliminate the consumption of heat from the host coal-fired power plant. Thirdly, the entire system will be more straightforward, compact, and modular, allowing any future scale-up to be implemented without technological difficulties. Finally, the amount of energy required to produce hydrogen will decline by around 25 %. [ABSTRACT FROM AUTHOR]