Alexandr Martaus

Natural fibrous clays—sepiolite (SEP) and palygorskite (PLG)—were evaluated as sustainable photocatalysts for UV-C hydrogen generation from aqueous methanol solution. Native and 24 h pre-irradiated samples were characterized by gas quantification, FTIR, SEM, AAS, and zeta-potential measurements and compared with TiO2 P25. PLG showed significant activation after irradiation: UV-C exposure removed carbonaceous residues and rearranged surface –OH groups, thereby improving channel accessibility and increasing H2 evolution to values comparable to P25. In contrast, SEP hydroxylated more strongly after irradiation and formed robust hydrogen bonds that stabilized methanol-derived intermediates and temporarily suppressed activity, even though the crystal structure remained stable. The results show that SEP and PLG respond to UV-C through different surface chemistry mechanisms, rather than changes in the crystal lattice. PLG is activated by surface cleaning and reorganization of hydroxyls, while SEP is inhibited by stabilization of intermediates and excessive hydroxylation. Overall, fibrous silicates appear to be affordable, robust, and tunable photocatalysts whose performance can be controlled by surface cleanliness and hydration.

The preparation of anodic TiO₂ nanotube layers has been performed using electrochemical anodization of Ti foil for 4 h at different voltages (from 0 V to 80 V). In addition, a TiO₂ thin layer has been also prepared using the sol–gel method. All the photocatalysts have been characterized by XRD, SEM, and DRS to investigate the crystalline phase composition, the surface morphology, and the optical properties, respectively. The performance of the photocatalyst has been assessed in versatile photocatalytic reactions including the reduction of N₂O gas and the oxidation of aqueous sulfamethoxazole. Due to their high specific surface area and excellent charge carriers transport, anodic TiO₂ nanotube layers have exhibited the highest N₂O conversion rate (up to 10% after 22 h) and the highest degradation extent of sulfamethoxazole (about 65% after 4 h) under UVA light. The degradation mechanism of sulfamethoxazole has been investigated by analyzing its transformation products by LC-MS and the predominant role of hydroxyl radicals has been confirmed. Finally, the efficiency of the anodic TiO₂ nanotube layer has been tested in real wastewater reaching up to 45% of sulfamethoxazole degradation after 4 h.

An alternative binder to calcium aluminate cement (CAC) was prepared by the sol-gel method. Chemically pure systems such as tetraethylorthosilicate (SiC₈H₂₀O₄) and nonahydrate of alumina nitrate (Al(NO₃)₃·9H₂O) were used as major raw materials. The manufacturing process of binder via solution is mentioned, and transitions in binder structure as a function of thermal treatment in the range between 85 and 1400 °C are described. Finally, binder efficiency was verified by its application in high-temperature concrete instead of calcium aluminate cement (CAC). Newly developed sol-gel binder was characterized by XRFS quantitative analyses, XRD diffraction, STA-DTA and TG analyses and the BET method. Samples of concrete which were based on natural bauxite raw material showed cold compressive strength of 42 MPa compared to the same material where a conventional CAC was applied, and samples reached cold compressive strength of 44 MPa.

Metakaolin (MK) prepared by the calcination of kaolin at 550 °C and fly ash (FA) from the combustion of black coal in a granulating boiler were used to prepare unfired ceramic bonding systems via the alkali activation process. A long-term stability of the mechanical properties of the prepared samples similar to the unfired ceramic systems was observed. The optimal metakaolin and fly ash ratio, the type of the activator (NaOH or water glass) and its concentration were evaluated after the hydration in: a) laboratory conditions; b) hydration box; and c) under the hydrothermal activation. Raw materials and the samples prepared by alkali activation process were characterized by XRD, XRF, TG/DTA, and FTIR methods. The mechanical properties of the prepared samples were tested using a compressive strength test after 2, 28 and 56 days of hydration. The compressive strengths of 16 and 24 MPa after 28 days of hydration were reached for FA samples activated with water glass. The alkali activation of MK was successful in the NaOH solution of the molar concentration above 5 M. The compressive strength values of metakaolin, activated hydrothermally and hydrated at laboratory conditions, reached 11.2 and 5.5 MPa, respectively, for 5 M activator of NaOH.

The effect of talc in the two mixtures with the representative sample of fly ash (Class F) was investigated at sintering temperatures of 1000, 1100, and 1200 °C. X-ray diffraction, thermal DTA/TGA, and mercury intrusion porosimetry analyses were applied to characterize the mineral phase transformation of talc and fly ash in cordierite ceramic. The influence of iron oxide on talc transformation to Fe-enstatite was verified by the simulated molecular models and calculated XRD patterns and the assumption of Fe-cordierite crystallization was confirmed. The fly ash mixtures with 10 mass% of talc in comparison with 30 mass% of talc at 1000 °C and 1100 °C showed higher linear shrinkage and lower porosity. At a temperature of 1200 °C, sintering expansion and larger pores in mullite and cordierite ceramics also containing sapphirine and osumilite demonstrated that magnesium in FA and Tc structure did not react with the other constituents to form crystalline cordierite. The ceramics produced in the present work using fly ash and talc have similar properties to the commercial ceramics produced at sintering temperatures higher than 1250 °C.

Direct decomposition of nitric oxide (NO) proceeds over Co–Mn–Al mixed oxides promoted by potassium. In this study, answers to the following questions have been searched: Do the properties of the K-promoted Co–Mn–Al catalysts prepared by different methods differ from each other? The K-precipitated Co–Mn–Al oxide catalysts were prepared by the precipitation of metal nitrates with a solution of K₂CO₃/KOH, followed by the washing of the precipitate to different degrees of residual K amounts, and by cthe alcination of the precursors at 500 °C. The properties of the prepared catalysts were compared with those of the best catalyst prepared by the K-impregnation of a wet cake of Co–Mn–Al oxide precursors. The solids were characterized by chemical analysis, DTG, XRD, N₂ physisorption, FTIR, temperature programmed reduction (H₂-TPR), temperature programmed CO₂ desorption (CO₂-TPD), X-ray photoelectron spectrometry (XPS), and the species-resolved thermal alkali desorption method (SR-TAD). The washing of the K-precipitated cake resulted in decreasing the K amount in the solid, which affected the basicity, reducibility, and non-linearly catalytic activity in NO decomposition. The highest activity was found at ca 8 wt.% of K, while that of the best K-impregnated wet cake catalyst was at about 2 wt.% of K. The optimization of the cake washing conditions led to a higher catalytic activity.