This paper is focused on development of the metal monolithic structure for total oxidation of toluene at low temperature. The well-adhered catalyst, based on the mixed oxides of manganese and nickel, is washcoated on the Al/Al₂O₃ plates as metallic support. For the comparison purposes, results observed for the manganese–nickel mixed oxide supported on the metallic monolith are compared with those obtained using powder type of the same catalyst. Prepared manganese–nickel mixed oxides in both configurations show remarkable low-temperature activity for the toluene oxidation. The reaction temperature T₅₀ corresponding to 50% of the toluene conversion is observed at temperatures of ca. 400–430 K for the powder catalyst and at ca. 450–490 K for the monolith configuration. The appropriate mathematical models, such as one-dimensional (1D) pseudo-homogeneous model of the fixed bed reactor and the 1D heterogeneous model of the metal monolith reactor, are applied to describe and compare catalytic performances of both reactors. Validation of the applied models is performed by comparing experimental data with theoretical predictions. The obtained results confirmed that the reaction over the monolithic structure is kinetically controlled, while in the case of the powder catalyst the reaction rate is influenced by the intraphase diffusion.

Manganese-doped ceria nanoparticles were prepared by hydrothermal synthesis and the prepared samples were thermally treated at 500 °C for 2 h. The samples were investigated using x-ray diffraction (XRD), high-resolution transmission electron microscopy (HR-TEM), energy-dispersive x-ray spectroscopy (EDS), N₂ adsorption and x-ray photoelectron spectroscopy (XPS). XRD revealed that nanocrystalline ceria is the main phase in all samples, while a romanechite-like phase (Na₂Mn₅O₁₀) appears in the sample doped with 30% of Mn. TEM coupled with EDS exposed the presence of the same phase in the sample doped with 20% Mn. While ceria particles have spherical morphology and particle size ranging from 4.3 to 9.2 nm, the rare crystals of the romanechite-like phase adopt a tubular morphology with a length of at least 1 μm. However, the decrease in the ceria lattice constant and the EDS spectra of the ceria nanoparticles clearly indicate that a substantial amount of manganese entered the ceria crystal lattice. Manganese doping has a beneficial impact on the specific surface area of ceria. XPS measurements reveal a decrease in the Ce³⁺/Ce³⁺ + Ce⁴⁺ content in the doped samples which is replaced by Mn³⁺. Moreover, a drastic increase in adsorbed oxygen is observed in the doped samples which is the consequence of the increase in Mn³⁺ species that promotes oxygen migrations to the surface of the sample. Compared to the pure sample, the doped samples showed significantly higher catalytic activity for the process of toluene oxidation.

The aim of this work was to develop hybrid TiO₂/ZIF-8 photocatalysts and test their activity for the removal of agricultural pollutants in water. The hybrid photocatalysts were prepared by an innovative method involving hydrothermal synthesis at 150 °C using a mechanochemically synthesized zeolitic imidazolate framework (ZIF-8) and titanium tetraisopropoxide as a titanium dioxide (TiO₂) precursor. Three composite photocatalysts with different mass fractions of titanium dioxide (5, 50, and 95 wt%) were synthesized and characterized, and their adsorption and photocatalytic properties investigated for the removal of imidacloprid. The equilibrium adsorption test showed that ZIF-8 is a good adsorbent and can adsorb 65% of the model component under the working conditions used in this work, while the hybrid photocatalysts can adsorb 1–3% of the model component. It is assumed that the adsorption is hindered by the TiO₂ layer on the surface of ZIF-8, which blocks the interactions of ZIF-8 and imidacloprid. A significant decrease in band gap energies (3.1–3.6 eV) was observed for the hybrid TiO₂/ZIF-8 photocatalysts compared to the values obtained with ZIF-8 (5 eV), depending on the mass fractions of TiO₂. The highest removal efficiency of imidacloprid was achieved with the hybrid photocatalysts containing 5 wt% TiO₂.

Due to its high solubility in water, a large amount of the neonicotinoid insecticide acetamiprid persisting in the soil of treated crops enters surface water or groundwater. The aim of this study was to investigate the photocatalytic degradation of acetamiprid in an aqueous medium. The experiments were carried out in an annular suspension reactor operating in recirculated batch mode and using a UV-A lamp as the radiation source. An appropriate modification of the commercial TiO₂-P25 photocatalyst was carried out to reduce its band gap energy and electron–hole recombination as well as to extend the visible light range of TiO₂. The photodegradation study was carried out using a three-factor two-stage Box–Behnken experimental design to investigate the main effects and interactions between the operating variables, such as solution pH, initial concentration of acetamiprid, and amount of photocatalyst. The efficiency of the processes was determined by high performance liquid chromatography. The first-order pseudo-reaction kinetic model, as a simplification of the models of Langmuir–Hinshelwood under conditions of relatively low acetamiprid concentration, was applied and the reaction rate constants were estimated. The results of the study showed that the initial concentration of the pollutant was the most influential factor for the photocatalytic degradation process. Using ANOVA analysis, a linear model was established to predict the system behaviour at different operating conditions. The highest conversion and rate constant of acetamiprid degradation were recorded in the experiment with the lowest tested concentration of acetamiprid (2 mg/L), the average concentration of photocatalyst (60 mg) and at pH 8. GRAPHICAL ABSTRACT