Investigating the Effects of the Physicochemical Properties of Cellulose-Derived Biocarbon on Direct Carbon Solid Oxide Fuel Cell Performance.

This paper presents a study of the characteristic effects of the physicochemical properties of microcrystalline cellulose and a series of biocarbon samples produced from this raw material through thermal conversion at temperatures ranging from 200 °C to 850 °C. Structural studies revealed that the biocarbon samples produced from cellulose had a relatively low degree of graphitization of the carbon and an isometric shape of the carbon particles. Based on thermal investigations using the differential thermal analysis/differential scanning calorimeter method, obtaining fully formed biocarbon samples from cellulose feedstock was possible at about 400 °C. The highest direct carbon solid oxide fuel cell (DC-SOFC) performance was found for biochar samples obtained via thermal treatment at 400-600 °C. The pyrolytic gases from cellulose decomposition had a considerable impact on the achieved current density and power density of the DC-SOFCs supplied by pure cellulose samples or biochars derived from cellulose feedstock at a lower temperature range of 200-400 °C. For the DC-SOFCs supplied by biochars synthesised at higher temperatures of 600-850 °C, the "shuttle delivery mechanism" had a substantial effect. The impact of the carbon oxide concentration in the anode or carbon bed was important for the performance of the DC-SOFCs. Carbon oxide oxidised at the anode to form carbon dioxide, which interacted with the carbon bed to form more carbon oxide. The application of biochar obtained from cellulose alone without an additional catalyst led to moderate electrochemical power output from the DC-SOFCs. The results show that catalysts for the reverse Boudouard reactions occurring in a biocarbon bed are critical to ensuring high performance and stable operation under electrical load, which is crucial for DC-SOFC development.

The Utilisation of Solid Fuels Derived from Waste Pistachio Shells in Direct Carbon Solid Oxide Fuel Cells.

The comprehensive results regarding the physicochemical properties of carbonaceous materials that are obtained from pistachio shells support their usage as solid fuels to supply direct carbon solid oxide fuel cells (DC-SOFCs). The influence of preparation conditions on variations in the chemical composition, morphology of the biochar powders, and degree of graphitization of carbonaceous materials were investigated. Based on structural investigations (X-ray diffraction analysis and Raman spectroscopy), it was observed that disordered carbon particles developed during the application of thermal treatments. The use of X-ray fluorescence enabled a comparative analysis of the chemical composition of the inorganic matter in biocarbon-based samples. Additionally, the gasification of carbonaceous-based samples vs. time at a temperature of 850 °C was investigated in a H2O or CO2 gas atmosphere. The analysis demonstrated the conversion rate of biochar obtained from pistachio shells to H2, CH4 and CO during steam gasification. The electrochemical investigations of the DC-SOFCs that were supplied with biochars obtained from pistachio shells were characterized by satisfactory values for the current and power densities at a temperature range of 700-850 °C. However, a higher power output of the DC-SOFCs was observed when CO2 was introduced to the anode chamber. Therefore, the impact of the Boudouard reaction on the performance of DC-SOFCs was confirmed. The chars that were prepared from pistachio shells were adequate for solid fuels for utilization in DC-SOFCs.

Samples of Ba1-xSrxCe0.9Y0.1O3-δ, 0 < x < 0.1, with Improved Chemical Stability in CO2-H2 Gas-Involving Atmospheres as Potential Electrolytes for a Proton Ceramic Fuel Cell.

Comparative studies were performed on variations in the ABO3 perovskite structure, chemical stability in a CO2-H2 gas atmosphere, and electrical conductivity measurements in air, hydrogen, and humidity-involving gas atmospheres of monophase orthorhombic Ba1-xSrxCe0.9Y0.1O3-δ samples, where 0 < x < 0.1. The substitution of strontium with barium resulting in Ba1-xSrxCe0.9Y0.1O3-δ led to an increase in the specific free volume and global instability index when compared to BaCe0.9Y0.1O3-δ. Reductions in the tolerance factor and cell volume were found with increases in the value of x in Ba1-xSrxCe0.9Y0.1O3-δ. Based on the thermogravimetric studies performed for Ba1-xSrxCe0.9Y0.1O3-δ, where 0 < x < 0.1, it was found that modified samples of this type exhibited superior chemical resistance in a CO2 gas atmosphere when compared to BaCe0.9Y0.1O3-δ. The application of broadband impedance spectroscopy enabled the determination of the bulk and grain boundary conductivity of Ba1-xSrxCe0.9Y0.1O3-δ samples within the temperature range 25-730 °C. It was found that Ba0.98Sr0.02Ce0.9Y0.1O3-δ exhibited a slightly higher grain interior and grain boundary conductivity when compared to BaCe0.9Y0.1O3-δ. The Ba0.95Sr0.05Ce0.9Y0.1O3-δ sample also exhibited improved electrical conductivity in hydrogen gas atmospheres or atmospheres involving humidity. The greater chemical resistance of Ba1-xSrxCe0.9Y0.1O3-δ, where x = 0.02 or 0.05, in a CO2 gas atmosphere is desirable for application in proton ceramic fuel cells supplied by rich hydrogen processing gases.

Assessment of mercury emissions into the atmosphere from the combustion of hard coal in a home heating boiler.

The purpose of the paper was to determine the factor of mercury emission into the atmosphere by households in Poland. Research for a home coal-fired boiler typical of Polish conditions was carried out, which was conducted throughout the heating season. On the basis of assessment of the quantity of coal burned and mercury content contained therein, as well as of the mercury content in bottom ash, chimney soot, boiler deposits and their quantities, annual mercury emissions and its factor of emission into the atmosphere were defined. It was defined that the mercury emission factor for the investigated case of a single-family house is at a level of 0.56 µg/MJ. It was shown that 41.4% of the mercury contained in coal burned in a home heating boiler is emitted into the atmosphere, 57.0% is adsorbed by chimney soot, 0.3% by boiler heater deposits and 1.3% passes into bottom ash. Annual mercury emissions into the atmosphere from the single-family house concerned was 79 mg. Mercury emissions can be significantly reduced by households by separating any overgrowths with pyrite from coal. The solution proposed would enable a reduction in annual mercury emissions into the atmosphere in Poland from the domestic user sector by 58.5% (0.351 Mg). The factor of emission of mercury into the atmosphere would be 0.23 µg/MJ.