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This work uses green sustainable reactions twice. Firstly, it is microwave synthesis: 2,4,6‐tribiphenyl‐4‐yl‐1,3,5‐triazine and similar compounds were prepared in a closed microwave reactor in n‐octane by the Friedel‐Crafts reaction. Second, a hybrid electrocatalyst for the highly demanded electrochemical reaction of nitrate reduction to ammonia (NO3RR) was prepared based on this material. This reaction has great potential to replace the energy‐intensive Haber‐Bosch process, and in addition, has independent value for the elimination of nitrate contamination of water resources. As shown in the work, microwave synthesis is an eco‐friendly method for the synthesis of complex organic compounds; fast, selective and with a high yield of the target product. The electrocatalyst deposited on the graphite electrode consisted of a layer of 2,4‐bis([1,1′‐biphenyl]‐4‐yl)‐6‐hydroxy‐1,3,5‐triazine and related compounds coated with cobalt oxide. The hybrid catalyst was firmly retained on the graphite electrode during NO3RR and the material showed impressive stability with almost no decrease in catalytic activity even after the fifth cycle. Both 2,4‐bis([1,1′‐biphenyl]‐4‐yl)‐6‐hydroxy‐1,3,5‐triazine and the catalyst based on this substance were characterized by SEM, XPS, XRD, UV‐vis spectra, cyclic (and linear) voltammetry, and chronoamperometry. This work can serve as a starting point for the development of stable and durable electrocatalysts for NO3RR using triazine derivatives. [ABSTRACT FROM AUTHOR]

Prospects for increasing the efficiency of heat and electric energy-generation and heat-and-power supply at thermal power plants obviously draw attention to such modern and innovative technologies as heat pumps. Heat pumps allow efficient redistribution of energy flows. The abundance of low-potential heat carriers and heat sources in the cycle arrangement of the thermal power plants operation requires modernization of production and increase of the fuel heat utilization factor, therefore, reduction of specific fuel consumption for the production of heat and electricity. This paper analyzes the influence and practicability of introducing heat pumps into the heating circuit of the return water of the heat network of power units with PT-80 and T-250 turbines. Heat pumps of various configurations provide invariant energy conversion factor and efficiency. To assess energy and economic efficiency, modeling of the operation of power units and calculation of heat pump circuits for various refrigerants are performed. The economic effect is represented in quarterly cash savings of operating costs.

Propylene is an important raw material for the production of many valuable compounds, especially polypropylene, the consumption of which continues to grow every year. The reaction of oxidative dehydrogenation of propane, where carbon dioxide is used as a mild oxidant, is a promising method for producing propylene. At the same time, the problem of utilization of greenhouse gas CO2 is partially solved. The synthesis and analysis of the physicochemical properties of mesoporous silicate MCM-41 and supported catalysts CrOx/MCM-41 prepared on its basis were carried out. These catalysts were prepared using incipient wetness impregnation. The support and catalysts were characterized by the methods of low-temperature nitrogen adsorption, TG-DTA, XRD, SEM, TPR-H2, UV/Vis diffuse reflectance spectroscopy, and small-angle X-ray scattering. It is shown that chromium is present in the samples simultaneously in the form of Cr3+ and Cr6+. The catalytic tests were performed in the range of 550–700 °C. The highest selectivity for propylene was observed for the 5%Cr/MCM-41 catalyst and was 76% at a temperature of 650 °C with a propane conversion of 20%. The deposited catalysts Cr/MCM-41 and Cr/SiO2 (Acros) were compared. The propylene selectivity for the MCM-41-supported catalyst was ~1.5 times higher than that for the SiO2-supported catalyst. [ABSTRACT FROM AUTHOR]

In this work, we studied the role of zinc in the composition of supported iron-containing catalysts for the hydrogenation of CO2. Various variants of incipient wetness impregnation of the support were tested to obtain catalyst samples. The best results are shown for samples synthesized by co-impregnation of the support with a common solution of iron and zinc precursors at the same molar ratio of iron and zinc. Catalyst samples were analyzed by various methods: Raman, DRIFT-CO, TPR-H2, XPS, and UV/Vis. The introduction of zinc leads to the formation of a mixed ZnFe2O4 phase. In this case, the activation of the catalyst proceeds through the stage of formation of the metastable wustite phase FeO. The formation of this wustite phase promotes the formation of metallic iron in the composition of the catalyst under the reaction conditions. It is believed that the presence of metallic iron is a necessary step in the formation of iron carbides—that is, active centers for the formation and growth of chain in the hydrocarbons. This leads to an increase in the activity and selectivity of the formation of hydrocarbons in the process of CO2 hydrogenation. [ABSTRACT FROM AUTHOR]

[Display omitted] For the first time, kinetic data on the decomposition of N 2 O over mixed oxide LaCoO 3 with a perovskite structure have been obtained. Bulk LaCoO 3 synthesized using microwave activation exhibited an increased intrinsic reaction rate with a 30 kJ mol–1 lower activation energy. Perovskite samples supported on ZrO 2 -La demonstrated lower intrinsic reaction rates due to the lower content of the LaCoO 3 phase, but the activation energies were also lower by 50–80 kJ mol–1. [ABSTRACT FROM AUTHOR]

This work uses green sustainable reactions twice. Firstly, it is microwave synthesis: 2,4,6-tribiphenyl-4-yl-1,3,5-triazine and similar compounds were prepared in a closed microwave reactor in n-octane by the Friedel-Crafts reaction. Second, a hybrid electrocatalyst for the highly demanded electrochemical reaction of nitrate reduction to ammonia (NO 3 RR) was prepared based on this material. This reaction has great potential to replace the energy-intensive Haber-Bosch process, and in addition, has independent value for the elimination of nitrate contamination of water resources. As shown in the work, microwave synthesis is an eco-friendly method for the synthesis of complex organic compounds; fast, selective and with a high yield of the target product. The electrocatalyst deposited on the graphite electrode consisted of a layer of 2,4-bis([1,1'-biphenyl]-4-yl)-6-hydroxy-1,3,5-triazine and related compounds coated with cobalt oxide. The hybrid catalyst was firmly retained on the graphite electrode during NO 3 RR and the material showed impressive stability with almost no decrease in catalytic activity even after the fifth cycle. Both 2,4-bis([1,1'-biphenyl]-4-yl)-6-hydroxy-1,3,5-triazine and the catalyst based on this substance were characterized by SEM, XPS, XRD, UV-vis spectra, cyclic (and linear) voltammetry, and chronoamperometry. This work can serve as a starting point for the development of stable and durable electrocatalysts for NO 3 RR using triazine derivatives., (© 2024 Wiley-VCH GmbH.)

The green and sustainable electrocatalytic conversion of nitrogen-containing compounds to ammonia is currently in high demand in order to replace the eco-unfriendly Haber-Bosch process. Model catalysts for the nitrate reduction reaction were obtained by electrodeposition of metal Co, Fe, and bimetallic Fe/Co nanoparticles from aqueous solutions onto a graphite substrate. The samples were characterized by the following methods: SEM, XRD, XPS, UV-vis spectroscopy, cyclic (and linear) voltammetry, chronoamperometry, and electrochemical impedance spectroscopy. In addition, the determination of the electrochemically active surface was also performed for all electrocatalysts. The best electrocatalyst was a sample containing Fe-nanoparticles on the layer of Co-nanoparticles, which showed a Faradaic efficiency of 58.2% (E = -0.785 V vs. RHE) at an ammonia yield rate of 14.6 μmol h -1 cm -2 (at ambient condition). An opinion was expressed to elucidate the mechanism of coordinated electrocatalytic action of a bimetallic electrocatalyst. This work can serve primarily as a starting point for future investigations on electrocatalytic conversion reactions to ammonia using model catalysts of the proposed type.