Calcined and acid-leached kaolin impregnated with Fe(NO₃)₃·9H₂O (6.6 wt. % Fe₂O₃) was developed as an inexpensive bifunctional catalyst for the slow fixed-bed pyrolysis of polypropylene (PP) and low-density polyethylene (LDPE). Experiments were run with catalyst-to-plastic mass ratios of 1:4, 1:2, and 1:1 in a quartz tube reactor heated from 25 to 800 °C. For PP, increasing the Fe/kaolin loading progressively raised non-condensable gas from 26 wt. % to 44 wt. % and drove liquid aromatics from 27.9% to 72.3%, while combined paraffins olefins fell to 2.5% and wax exhibited a 46 → 24 → 36 wt. % trend. In contrast, LDPE at a 1:4 ratio already yielded 56 wt. % oil and only 22 wt. % wax; further catalyst addition mainly enhanced CH₄/CO-rich pyrolysis gas (PyGas) and char without substantially boosting aromatics. Gas analysis confirmed that Fe₂O₃ reduction and kaolin de-hydroxylation generated in situ H₂O, CO, and H₂. Given the catalyst’s low cost, regenerability, and ability to valorize the two most abundant waste polyolefins within the same reactor, the process offers a scalable route to flexible fuel and gas production from mixed plastic streams.

The development and improvement of methods for the synthesis of environmentally friendly catalysts based on base metals is currently an urgent and promising task of modern catalysis. Catalysts based on nanoscale magnetite and maghemite have fast adsorption–desorption kinetics and high chemical activity. The purpose of this work is to obtain magnetic composites, determine their physicochemical characteristics and verify their activity in the process of liquid-phase oxidation of phenol with oxygen. Magnetic nanocomposites were obtained by chemical co-deposition of salts of ferrous and trivalent iron. The synthesized magnetic composites were studied by X-ray diffractometry, energy dispersive X-ray fluorescence and Mössbauer spectroscopy, IR-Fourier spectroscopy and elemental analysis. To increase the catalytic activity in oxidative processes, the magnetite surfaces were modified using cobalt nitrate salt. Further, CoFe₂O₄ was stabilized by adding polyethylenimine (PEI) as a surfactant. Preliminary studies of the oxidation of phenol with oxygen, as the most typical environmental pollutant were carried out on the obtained Fe₃O₄, CoFe₂O₄, CoFe₂O₄/PEI catalysts. The spectrum of the reaction product shows the presence of CH in the aromatic ring and double C=C bonds, stretching vibrations of the C=O groups of carbonyl compounds; the band at 3059 cm⁻¹ corresponds to the presence of double C=C bonds and the band at 3424 cm⁻¹ to hydroquinone compounds. The band at 1678 cm⁻¹ and the intense band at 1646 cm⁻¹ refer to vibrations of the C=O bonds of the carbonyl group of benzoquinone. Peaks at 1366 cm⁻¹ and 1310 cm⁻¹ can be related to the vibrations of C–H and C–C bonds of the quinone ring. Thus, it was demonstrated that produced magnetic composites based on iron oxide are quite effective in the oxidation of phenol with oxygen.

In this work, the synthesis of magnetite nanoparticles and catalysts based on it stabilized with silicon and aluminum oxides was carried out. It is revealed that the stabilization of the magnetite surface by using aluminum and silicon oxides leads to a decrease in the size of magnetite nanocrystals in nanocomposites (particle diameter less than ~10 nm). The catalytic activity of the obtained catalysts was evaluated during the oxidation reaction of phenol, pyrocatechin and cresol with oxygen. It is well known that phenolic compounds are among the most dangerous water pollutants. The effect of phenol concentration and the effect of temperature (303–333 K) on the rate of oxidation of phenol to Fe₃O₄/SiO₂ has been studied. It has been determined that the dependence of the oxidation rate of phenol on the initial concentration of phenol in solution is described by a first-order equation. At temperatures of 303–313 K, incomplete absorption of the calculated amount of oxygen is observed, and the analysis data indicate the non-selective oxidation of phenol. Intermediate products, such as catechin, hydroquinone, formic acid, oxidation products, were found. The results of UV and IR spectroscopy showed that catalysts based on magnetite Fe₃O₄ are effective in the oxidation of phenol with oxygen. In the UV spectrum of the product in the wavelength range 190–1100 nm, there is an absorption band at a wavelength of 240–245 nm and a weak band at 430 nm, which is characteristic of benzoquinone. In the IR spectrum of the product, absorption bands were detected in the region of 1644 cm⁻¹, which is characteristic of the oscillations of the C=O bonds of the carbonyl group of benzoquinone. The peaks also found at 1353 cm⁻¹ and 1229 cm⁻¹ may be due to vibrations of the C-H and C-C bonds of the quinone ring. It was found that among the synthesized catalysts, the Fe₃O₄/SiO₂ catalyst demonstrated the greatest activity in the reaction of liquid-phase oxidation of phenol.

The purpose of this work was to create magnetic nanocatalysts that could be used for the oxidation of organic water pollutants – phenol and its derivatives – and to determine the physicochemical characteristics of the catalysts. The development of such active nanocomposite catalysts would solve the environmental problem in the Republic of Kazakhstan in the field of wastewater treatment from organic impurities, including phenols, and would also contribute to the subsequent creation of domestic production of oxygen-containing compounds, since almost the entire spectrum of oxygen-containing compounds for various industries is imported into the Republic. Nanosized magnetic composites based on Fe and Co were obtained by chemical deposition, in some cases, using polyethyleneimine and polyvinylpyrrolidone. It was shown that the interaction between nanoparticles and the polymer takes place in the case of a CoFe2O4 catalyst stabilized with polyvinylpyrrolidone or polyethyleneimine, which may indicate the efficient formation of nanocomposites. According to the IR study, for the CoFe2O4 nanocomposite stabilized with polyvinylpyrrolidone, the absorption bands at 735, 663, 649, 626 cm–1 are natural vibrations for the composite nanoparticles embedded in a polyvinylpyrrolidone matrix. The synthesized nanocomposites were tested in the oxidation of phenol with oxygen. The results demonstrate that the catalysts are promising both for the purification of industrial wastewater from phenol and for the synthesis of oxygen-containing compounds in the liquid phase under mild conditions.

The development of new catalytic systems based on cobalt and iron compounds for the production of oxygen-containing compounds is an urgent task of chemical technology. The purpose of this work is the synthesis of CoFe₂O₄ stabilized with polyvinylpyrrolidone (PVP), the study of the catalyst by physico-chemical research methods, and the determination of the effectiveness of the CoFe₂O₄/PVP catalyst in the phenol oxidation reaction. In this work, magnetic composites CoFe₂O₄ and CoFe₂O₄ stabilized with polyvinylpyrrolidone were synthesized by co-deposition. A comparison of the characteristics of the properties of the synthesized cobalt (II) ferrite (CoFe₂O₄) and the composite material CoFe₂O₄/PVP based on it is carried out. The obtained samples were examined using X-ray phase analysis (XRD), the Debye–Scherrer method, scanning electron microscopy (SEM), Mossbauer and IR Fourier spectroscopy, as well as thermogravimetric analysis (TGA). The textural properties were determined based on the analysis of nitrogen isotherms. The catalytic properties of the synthesized materials in the process of phenol oxidation in the presence of hydrogen peroxide are considered. The analysis of the reaction mixtures by HPLC obtained by the oxidation of phenol in the presence of a CoFe₂O₄/PVP catalyst showed a decrease in the concentration of phenol in the first 15 min of the process (by 55–60%), and then within 30 min, the concentration of phenol decreased to 21.83%. After 2 h of the process, the conversion of phenol was already more than 95%. The final sample after the reaction contained 28% hydroquinone and 50% benzoquinone. It was found that the synthesized magnetic composites exhibit catalytic activity in this process.

It is known that highly efficient catalysts for the catalytic oxidation of aromatic hydrocarbons can be obtained based on magnetic nanoparticles. The development of nanosized magnetically controlled catalysts for the oxidation of aromatic hydrocarbons with oxygen deserves especially close attention in the territory of the Republic of Kazakhstan, which does not have its own industrial production of oxygen-containing compounds. The aim of this work is to create catalysts based on Fe and Co nanoparticles stabilized with polymers: polyvinylpyrrolidone, chitosan, and polyethylenimine, study them by methods of physico-chemical research, and conduct preliminary tests of catalysts to predict their effectiveness. Magnetic nanoparticles were prepared by the co-precipitation method. Based on the results of the SEM analysis, it was concluded that polymers form composites together with metal nanocrystals. According to preliminary data, the most efficient oxidation of phenol in a non-flowing glass gradient-free thermostated duck-type reactor occurs on Fe₃O₄/chitosan, with the phenol conversion being 55–60%. Tests on the oxidation of phenol with oxygen showed a favorable prognosis for the use of such catalysts for the oxidative conversion of aromatic hydrocarbons in order to obtain valuable intermediates.