Although the potential of natural minerals for purification of liquid radioactive wastes (LRW) from radionuclides has been widely studied, the use of hybrid polymer composites made of zeolite is still rather scarce. This article reports on the preparation of zeolite-based hybrid polymer composites using the in situ polymerization technique in the body of mineral matrix and its intercalated with copper ferrocyanide (CuFC) forms. This hybrid polymer composites have shown unique and enhanced properties for the removal of micropollutants from wasted water as compared to the individual mineral. The change in conventional properties of two mixed minerals, such as zeolite and bentonite, and their intercalated with CuFC forms were probed using techniques such as scanning electron microscopy (SEM), X-ray diffraction (XRD), Mössbauer spectroscopy (MS) and FT-IR analysis. The totality of analysis showed a coexistence of intercalated and percolated zeolite phases. The hybrid polymer composites exhibited both adsorption and ion-exchange properties in the removal of ^134,137Cs⁺, ^57,60Co²⁺ and ⁸⁵Sr²⁺ radionuclides from LRW.

This article presents a study of the synthesis and characterization of new biphasic hybrid composite materials consisting of intercalated complexes (ICC) of natural mineral bentonite with copper hexaferrocyanide (phase I), which are incorporated into the bulk of the polymer matrix (phase II). It has been established that the sequential modification of bentonite with copper hexaferrocyanide and introduction of acrylamide and acrylic acid cross-linked copolymers into its volume by means of in situ polymerization promote the formation of a heterogeneous porous structure in the resulting hybrid material. The sorption abilities of prepared hybrid composite toward radionuclides of liquid radioactive waste (LRW) have been studied, and the mechanism for binding radionuclide metal ions with the components of the hybrid composition have been described.

The article investigates the potential for producing hydrogen by combining the methods of water splitting under cavitation and the chemical activation of aluminum in a high-speed cavitation–jet flow generated by a specialized hydrodynamic reactor. The process of cavitation and water spraying causes the liquid heating itself until it reaches saturated vapor pressure, resulting in the creation of vapor–gaseous products from the splitting of water molecules. The producing of vapor–gaseous products can be explained through the theory of non-equilibrium low-temperature plasma formation within a high-speed cavitation–jet flow of fluid. Special focus is also given to the interactions occurring at the interface boundary phase of aluminum and liquid under cavitation condition. The primary solid products formed on aluminum surfaces are bayerite, copper oxides (I and II), iron carbide, and a compound of magnesium oxides and aluminum hydroxide. A high hydrogen yield of 60% was achieved when using a 0.1% sodium hydroxide solution as a working liquid compared to demineralized water. Moreover, hydrogen methane was also detected in the volume of the vapor–gas mixture, which could be utilized to address the challenges of decarbonization and the recycling of aluminum-containing solid industrial and domestic waste. This work provides a contribution to the study of the mechanism of hydrogen generation by cavitation–jet processing of water and aqueous alkali solutions, in which conditions are created for double cavitation in the cavitation–jet chamber of the hydrodynamic reactor.

Although the potential of natural minerals for purification of liquid radioactive wastes (LRW) from radionuclides has been widely studied, the use of hybrid polymer composites made of zeolite is still rather scarce. This article reports on the preparation of zeolite based hybride polymer composites using the in-situ polymerization technique in the body of mineral matrix and its intercalated with copper ferrocyanide (CuFC) forms. This hybrid polymer composites have shown unique and enhanced properties as compared to the individual mineral. The change in conventional properties of two mixed minerals such as zeolite and bentonite and their intercalated with CuFC forms were probed using technics such as scanning electron microscopy (SEM), X-ray diffraction (XRD), Mossbauer spectroscopy (MS) and FT-IR analysis. The totality of analysis showed a coexistence of intercalated and percolated zeolite phases. The hybrid polymer composites exhibited both adsorption and ion-exchangr properties in removal of radionuclides from LRW.

This study investigates the feasibility of treating acidic gases produced in oilfields using a novel method that combines cavitation-jet reactor (CJR) technology with electric arc discharge (EAD). The integration of these two approaches enhances the ionization process by converting neutral gas molecules into chemically reactive ion-radical and radical fragments. These highly reactive species eventually recombine, creating new chemical compounds and simpler molecules from incoming acid gas and water vapor. Theoretical validation and experimental demonstration have revealed possible mechanisms and pathways of low-temperature plasma-chemical processes resulting from the synergistic effects of cavitating-jet flow and arc discharge on the molecular degradation of neutral gaseous molecules, such as hydrogen sulfide and carbon dioxide in water vapor, which lead to the generation of new compounds. Research indicates that the most effective method for processing associated petroleum gas (APG) involves minimizing the sequential nature of chemical reactions in low-temperature non-equilibrium plasma environments, thus eliminating the need for costly and complex catalysts. Additionally, studies have shown that the cavitation-jet flow of a gas–vapor–liquid mixture, when combined with an electric arc discharge in the truncated region of the low-temperature plasma of CJR, results in the synthesis of hydrogen, two forms of S₈ (S₈^I and S₈^II), crystalline carbon, and its organic derivatives containing oxygen and nitrogen, specifically methanol, ethanol, acetone, and acetonitrile. The data obtained suggest that the generation of low-temperature plasma in the cavitation-jet chamber, induced by an electric discharge, is essential for the production of reaction products, such as hydrogen, sulfur, and oxygen- and nitrogen-containing derivatives of organic carbon, when water vapor and acid gas molecules traverse the reactor.

The synthesis, structure and features of the formation of biphasic hybrid polymer compositions based on natural ionite (bentonite – BT), its intercalated complex (ICC) with a solid solution of copper ferrocyanide K_4-хCu_x[Fe(CN)₆] and a synthetic rare cross-linked acrylamide-acrylic acid copolymer were studied. The mechanism of formation of biphasic intercalated and percolated structures was analyzed by means of X-ray diffraction, X-ray fluorescence analysis, IR-Fourier spectroscopy and stress-strain curves. It is shown that the impregnation of the mineral bentonite filler into the polymer matrix, including its intercalated complex {BT:K_4-xCu_x[Fe(CN)₆]} is accompanied by an increase of non-uniformity of the structure of the hybrid composite material. It has been established that the main factor characterizing the deformation stability of the composite is the adhesive strength at the interface between the mineral filler and the polymer matrix. Under uniaxial tension of the P[AA-AA]{BT} composition and the percolated complex P[AA-AA]{BT:K_4-xCu_x[Fe(CN)₆]} their internal structure is rearranged resulting in stretching of agglomerates of solid fillers along polymer chains, which is determined by the adhesion force between polymer chains and mineral particles at the phase boundary. It is proposed to consider such biphasic hybrid composite materials as a promising class of interpenetrating networks with valuable applied properties.