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Heat storage is an emerging field of research, and, therefore, new materials with enhanced properties are being developed. Examples of phase change materials that provide high heat storage are inorganic salts and salt mixtures. They are commonly used for industrial applications due to their high operational temperature and latent heat. These parameters can be modified by combining different types of salts. This paper presents the experimental study of the impact of the composition of binary salts on their thermophysical properties. Unlike the literature data, this article provides a detailed analysis of the phase change process in both directions: solid–liquid and liquid–solid. The results indicate that the highest latent heat was observed for a 70% NaNO3 content in the NaNO3–KNO3 mixture. Therefore, when this salt is used for heat storage, the most favorable choice is a 70:30 ratio, which provides the highest heat storage density and the lowest phase transition temperature. In the case of the NaNO3–NaNO2 mixture, the highest value of latent heat occurs for a ratio of 80:20, resulting in phase transition temperatures of 267.0 °C for the solid–liquid transition, and 253.5 °C for the liquid–solid transition. For heat storage applications, it is recommended to use pure NaNO2 salt instead of the NaNO3–NaNO2 mixture. [ABSTRACT FROM AUTHOR]

Biodiesel manufacturing frequently employs sustainable materials like soybeans, microorganisms, palm extract, jatropha plant, and recycled frying oils. The expansion of biodiesel manufacturing has escalated the volume of waste byproducts, encompassing glycerin and non-glycerin organic matter (MONG), jointly known as raw glycerin. MONG is characterized by a low calorific value, a high autoignition temperature, and significant viscosity at room temperature. As a waste product, it negatively affects the natural environment due to the lack of viable disposal methods. Hence, there is a need for its conversion into high-calorific gaseous fuel with significantly less environmental impact. One of the methods for converting MONG into gaseous fuel is the pyrolysis process. This study describes the pyrolytic conversion of MONG conducted on a test stand consisting of a rotating chamber with a shell filled with liquid lead as a heating medium. Based on the measurements and balance calculations, the amount of heat required to preserve the autothermal process was determined. The calorific value and composition of the pyrolytic gas were measured, revealing that 70% of the gas involves compounds characterized by a high calorific value. As a result, the calorific value of dry, purified gas equals 35.07 MJ/kg. A life cycle assessment has been conducted, in order to determine if the produced gaseous fuel matches sustainable development criteria. MONG-based gas is a sustainable replacement of, e.g., natural gas, lignite, or hard coal; however, it allows us to avoid 233–416 kg/h CO2 emissions per 1 MWt of heat. [ABSTRACT FROM AUTHOR]

We present a DFT analysis of the role of the Cu-Ni synergistic effect for the CO2 reduction to C2H4, in comparison to the pure Cu catalyst. The analysis is focused on the thermodynamic stability of reactive intermediates along the proposed pathway of C2 species formation. We have observed that the potential needed for the reaction decreases with the addition of Ni in the investigated model. In addition, we have observed the differences in the preferred pathway based on the significant differences in stability of the reactive intermediates depending on th Cu:Ni ratio. The results suggest that despite the fact the Cu surface is always exposed, and it is the only one that is able to directly interact with the intermediates, the presence of the Ni in the underlying sections of the crystal is significant enough to change the mechanism of the reaction. [ABSTRACT FROM AUTHOR]

The paper presents studies on the impact of the process of condensation of water vapour on the process of cleaning of flue gases from acidic compounds. The measurements were carried out on a pilot-scale plant for waste heat recovery from flue gases, taking into account the process of condensation of the water vapour contained in them. The plant was connected to a lignite-fired power unit with a capacity of 360 MW located at PGE GiEK S.A., Bełchatów Power Plant Branch. The impact of the condensation of water vapour on the reduction of sulphur, chlorine and fluorine forming acidic compounds was examined. The studies show that the condensation process is conducive to removal of acidic compounds from flue gases.

Reaction mechanisms for the catalytic hydrogenation of CO2 by faujasite-supported Ir4 clusters were studied by periodic DFT calculations. The reaction can proceed through two alternative paths. The thermodynamically favoured path results in the reduction of CO2 to CO, whereas the other, kinetically preferred channel involves CO2 hydrogenation to formic acid under water-free conditions. Both paths are promoted by catalytic amounts of water confined inside the zeolite micropores with a stronger promotion effect for the reduction path. Co-adsorbed water facilitates the cooperation between the zeolite Brønsted acid sites and Ir4 cluster by opening low-energy reaction channels for CO2 conversion. [ABSTRACT FROM AUTHOR]