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This perspective describes different schemes of power systems integration for various process technology in oil refining and petrochemistry with a focus on distillation. An overview is given of different methods of gas turbines and turboexpanders. Application of the organic Rankine cycle is considered for distillation processes, especially for unconventional schemes, which are integrated into the main process as stand-alone ones, as well when the working fluid of an energy system is a process stream per se. Despite a more complex structure and potential interference with the main process, such schemes are advantageous in terms of more efficient equipment utilization. Integration of turboexpanders in separation processes and in reactor units can improve energy generation efficiency 2–3 fold compared with traditional schemes of energy generation from fossil feedstock. From the economic viewpoint for distillation columns, total annual costs can be decreased by ca. 5–15% with the specific costs of additional generated electricity being very close to the costs of a heating utility.

Rare-earth orthoferrites have found wide application in thermocatalytic reduction-oxidation processes. Much less attention has been paid, however, to the production of CeFeO3, as well as to the study of its physicochemical and catalytic properties, in particular, in the promising process of CO2 utilization by hydrogenation to CO and hydrocarbons. This study presents the results of a study on the synthesis of CeFeO3 by solution combustion synthesis (SCS) using various fuels, fuel-to-oxidizer ratios, and additives. The SCS products were characterized by XRD, FTIR, N2-physisorption, SEM, DTA–TGA, and H2-TPR. It has been established that glycine provides the best yield of CeFeO3, while the addition of NH4NO3 promotes an increase in the amount of CeFeO3 by 7–12 wt%. In addition, the synthesis of CeFeO3 with the participation of NH4NO3 makes it possible to surpass the activity of the CeO2–Fe2O3 system at low temperatures (300–400 °C), as well as to increase selectivity to hydrocarbons. The observed effects are due to the increased gas evolution and ejection of reactive FeOx nanoparticles on the surface of crystallites, and an increase in the surface defects. CeFeO3 obtained in this study allows for achieving higher CO2 conversion compared to LaFeO3 at 600 °C.

The study on influence of initial SiO 2 /Al 2 O 3 ratio and approaches to precursor mixing (conventional mixing with magnetic stirrer and overhead mixing with ultrasonication (US)) on phase, texture and acidity of SAPO-34 and catalytic performance in methanol-to-olefin (MTO) process is presented. Contribution of the amorphous phase in the catalysts were determined using neural network via counting cubic (crystalline) and spherical (amorphous) particles in SEM images. We have found out that ultrasonication pre-treatment improves the crystallinity of SAPO-34 crystals and facilitates silicon incorporation into AlPO framework at higher SiO 2 /Al 2 O 3 ratio. Acidity of samples synthesized with US pre-treatment is increased comparing with corresponding samples synthesized without US pre-treatment. US-treated catalyst lifetime is also enhanced. As a result, total olefin yield is higher on US-treated catalysts comparing with corresponding SiO 2 /Al 2 O 3 ratio of non-treated ones.

An evaporation-deposition coating method for coating the inner surface of long (>1 m) quartz tubes of small diameter has been studied by the introduction of two-phase (gas-liquid) flow with the gas core flowing in the middle and a thin liquid film of synthesis sol flowing near the hot tube wall. The operational window for the deposition of continuous titania coatings has been obtained. The temperature range for the deposition of continuous titania coatings is limited to 105–120 °C and the gas flow rate is limited to the range of 0.4–1.0 L min−1. The liquid flow rate in the annular flow regime allows to control the coating thickness between 3 and 10 micron and the coating porosity between 10% and 20%. By increasing the liquid flow rate, the coating porosity can be substantially reduced. The coatings were characterized by X-ray diffraction, N2 chemisorption, thermogravimetric analysis, and scanning electron microscopy. The coatings were tested in the photocatalytic decomposition of methylene blue and rhodamine B under UV-light and their activity was similar to that of a commercial P25 titania catalyst.

Plasma-assisted dry reforming of methane (DRM) is considered as a potential way to convert natural gas into fuels and chemicals under near ambient temperature and pressure; particularly for distributed processes based on renewable energy. Both catalytic and photocatalytic technologies have been applied for DRM to investigate the CH4 conversion and the energy efficiency of the process. For conventional catalysis; metaldoped Ni-based catalysts are proposed as a leading vector for further development. However; coke deposition leads to fast deactivation of catalysts which limits the catalyst lifetime. Photocatalysis in combination with non-thermal plasma (NTP), on the other hand; is an enabling technology to convert CH4 to more reactive intermediates. Placing the catalyst directly in the plasma zone or using post-plasma photocatalysis could generate a synergistic effect to increase the formation of the desired products. In this review; the recent progress in the area of NTP-(photo)catalysis applications for DRM has been described; with an in-depth discussion of novel plasma reactor types and operational conditions including employment of ferroelectric materials and nanosecond-pulse discharges. Finally, recent developments in the area of optical diagnostic tools for NTP, such as optical emission spectroscopy (OES), in-situ FTIR, and tunable diode laser absorption spectroscopy (TDLAS), are reviewed.

Rare-earth orthoferrites have found wide application in thermocatalytic reduction-oxidation processes. Much less attention has been paid, however, to the production of CeFeO , as well as to the study of its physicochemical and catalytic properties, in particular, in the promising process of CO utilization by hydrogenation to CO and hydrocarbons. This study presents the results of a study on the synthesis of CeFeO by solution combustion synthesis (SCS) using various fuels, fuel-to-oxidizer ratios, and additives. The SCS products were characterized by XRD, FTIR, N -physisorption, SEM, DTA-TGA, and H -TPR. It has been established that glycine provides the best yield of CeFeO , while the addition of NH NO promotes an increase in the amount of CeFeO by 7-12 wt%. In addition, the synthesis of CeFeO with the participation of NH NO makes it possible to surpass the activity of the CeO -Fe O system at low temperatures (300-400 °C), as well as to increase selectivity to hydrocarbons. The observed effects are due to the increased gas evolution and ejection of reactive FeO nanoparticles on the surface of crystallites, and an increase in the surface defects. CeFeO obtained in this study allows for achieving higher CO conversion compared to LaFeO at 600 °C.

Rare-earth orthoferrites have found wide application in thermocatalytic reduction-oxidation processes. Much less attention has been paid, however, to the production of CeFeO[sub.3] , as well as to the study of its physicochemical and catalytic properties, in particular, in the promising process of CO[sub.2] utilization by hydrogenation to CO and hydrocarbons. This study presents the results of a study on the synthesis of CeFeO[sub.3] by solution combustion synthesis (SCS) using various fuels, fuel-to-oxidizer ratios, and additives. The SCS products were characterized by XRD, FTIR, N[sub.2] -physisorption, SEM, DTA–TGA, and H[sub.2] -TPR. It has been established that glycine provides the best yield of CeFeO[sub.3] , while the addition of NH[sub.4] NO[sub.3] promotes an increase in the amount of CeFeO[sub.3] by 7–12 wt%. In addition, the synthesis of CeFeO[sub.3] with the participation of NH[sub.4] NO[sub.3] makes it possible to surpass the activity of the CeO[sub.2] –Fe[sub.2] O[sub.3] system at low temperatures (300–400 °C), as well as to increase selectivity to hydrocarbons. The observed effects are due to the increased gas evolution and ejection of reactive FeO[sub.x] nanoparticles on the surface of crystallites, and an increase in the surface defects. CeFeO[sub.3] obtained in this study allows for achieving higher CO[sub.2] conversion compared to LaFeO[sub.3] at 600 °C.