Sulfur-doped TiO₂ (S-TiO₂) composites with reduced graphene oxide (rGO), wt. % of rGO equal to 0.5%, 2.75%, and 5.0%, were prepared by a one-pot solvothermal procedure. The aim was to improve photocatalytic performance in comparison to TiO₂ under simulated solar irradiation for the treatment of diclofenac (DCF) in aqueous medium. The obtained composites were characterized for physical-chemical properties using thermogravimetric analysis (TGA), X-ray diffractograms (XRD), Raman, scanning electron microscopy (SEM)/energy dispersive X-ray (EDX), Brauner Emmett Teller (BET), and photoluminescence (PL) analyses, indicating successful sulfur doping and inclusion of rGO. Sulfur doping and rGO have successfully led to a decrease in photogenerated charge recombination. However, both antagonistic and synergistic effects toward DCF treatment were observed, with the latter being brought forward by higher wt.% rGO. The composite with 5.0 wt.% rGO has shown the highest DCF conversion at pH 4 compared to that obtained by pristine TiO₂, despite lower DCF adsorption during the initial dark period. The expected positive effects of both sulfur doping and rGO on charge recombination were found to be limited because of the subpar interphase contact with the composite and incomplete reduction of the GO precursor. Consequent unfavorable interactions between rGO and DCF negatively influenced the activity of the studied S-TiO₂/rGO photocatalyst under simulated solar irradiation.

A green method for depositing a CuO layer with good adhesion and a large surface area on a support of activated alumina (Al₂O₃) was evaluated. The relatively simple method consists of adsorption of a copper salt on the surface of Al₂O₃, formation of Cu(OH)₂, and subsequent decomposition of the hydroxide to CuO. The XRD confirmed that the deposited photocatalyst crystalized at low temperatures (80 °C). Furthermore, BET measurements show a surface area of about 90 m²/g. The large surface area is the result of the speed of the conversion and decomposition reactions. The photokilling properties of the prepared photocatalyst were evaluated using E. coli cells and the leaching of copper ions was determined using ICP-MS. The photocatalytic efficiency was also evaluated by the degradation of an organic azo dye. The prepared photocatalyst shows good activity in the purification and disinfection of treated water. The described method is economical, fast, and can be considered green, since the only byproducts are water and NaCl.

When wood is thermally modified, several chemical reactions take place that change the chemical and physical properties of the wood. These changes correlate with the degree of modification, which is mostly a function of the temperature and duration of modification, and consequently with the mass loss during this process. There is a lack of standardised quality control to verify the degree of heat treatment of wood and thus its quality. One of the possible methods to check the degree of thermal modification of a particular type of wood is thermogravimetry (TG). It is based on the assumption that processes that did not take place during thermal modification continue when the TG experiment is carried out. In this method, calibration curves have to be established based on TG measurements of standard samples that have been thermally modified at different temperatures and whose mass loss during modification is known. The calibration curves show the mass loss during the TG measurement as a function of the mass loss during the previous thermal modification. The course of thermal decomposition during the TG measurements is influenced by many parameters, such as the mass of the sample, the heating rate, the atmosphere in which the measurement takes place, and the shape of the crucible in which the sample is placed. In this paper, the influence of these parameters on the calibration curves was investigated. We have focused on oak wood. The best parameters result in a calibration curve with the largest correlation coefficient R² and the highest slope of the line k. On this basis, we can determine the mass loss during the thermal modification of unknown samples of the same wood species under the same measurement conditions.

Sustainable hydrogen production is one of the main challenges today in the transition to a green and sustainable economy. Photocatalytic hydrogen production is one of the most promising technologies, amongst which BiVO₄-based processes are highly attractive due to their suitable band gap for solar-driven processes. However, the performance of BiVO₄ alone in this role is often unsatisfactory. Herein we report the improvement of BiVO₄ performance with reduced graphene oxide (rGO) as a co-catalyst for the photoelectrochemical water splitting (PEC-WS) in the presence of simple functionalized benzene derivatives (SFBDs), i.e., phenol (PH), benzoic acid (BA), salicylic acid (SA), and 5-aminosalicylic acid (5-ASA) as potential photogenerated hole scavengers from contaminated wastewaters. Linear sweep voltammetry and chronoamperometry, along with electrochemical impedance spectroscopy were utilized to elucidate PEC-WS performance under illumination. rGO has remarkably improved the performance of BiVO₄ in this role by decreasing photogenerated charge recombination. In addition, 5-ASA greatly improved current densities. After 120 min under LED illumination, 0.53 μmol of H₂ was produced. The type and concentration of SFBDs can have significant and at times opposite effects on the PEC-WS performance of both BiVO₄ and rGO-BiVO₄.

Wider application of BiVO₄ (BVO) for photocatalytic water treatment is primarily limited by its modest photocatalytic effectiveness, despite its appropriately narrow band gap for low-cost, sunlight-facilitated water treatment processes. In this study, we have photomodified an isotype BVO, consisting of a tetragonal zircon and monoclinic scheelite phase, with Fe (Fe@BVO) and Ag (Ag@BVO) ionic precursors under UV illumination in an aqueous ethanol solution in order to assess their effect on the opto-electronic properties and effectiveness for the removal of ciprofloxacin (CIP). Fe@BVO failed to demonstrate enhanced effectiveness over pristine BVO, whereas all Ag@BVO achieved improved CIP degradation, especially 1% Ag@BVO. At pH 4 and 6, 1% Ag@BVO demonstrated nearly 24% greater removal of CIP than BVO alone. Photomodification with Fe created surface oxygen vacancies, as confirmed by XPS and Mott–Schottky analysis, which facilitated improved electron mobility, although no distinct Fe-containing phase nor Fe-doping was detected. On the other hand, the introduction of mid-band gap states by oxygen vacancies decreased the reducing power of the photogenerated electrons as the flat band potentials were shifted to more positive values, thus likely negatively impacting superoxide formation. In contrast, Ag-photomodification (Ag@BVO) resulted in the formation of Ag₂O/AgO and Ag nanoparticles on the surface of BVO, which, under illumination, generated hot electrons by surface plasmon resonance and enhanced the mobility of photogenerated electrons. Our research underscores the pivotal role of photogenerated electrons for CIP degradation by BiVO₄-based materials and emphasizes the importance of appropriate band-edge engineering for optimizing contaminant degradation.

The application of TiO2 photocatalysis in various environmental fields has been extensively studied in the last decades due to its ability to induce the degradation of adsorbed organic pollutants. In the present work, TiO2 powders doped and co-doped with sulfur and nitrogen and modified with platinum were prepared by particulate sol-gel synthesis. PXRD measurements revealed that the replacement of HCl with H2SO4 during synthesis reduced the size of the crystallites from ~ 30 nm to ~20 nm, increasing the surface area from ~44 m2/g to ~80 m2/g. This is consistent with the photocatalytic activity of the samples and the measured photocurrent behavior of the photocatalysts. The results showed that the properties of the powders (i.e., surface area, crystallite size, photocurrent behavior) depend strongly not only on the type but also on the amount of acid and dopants used in the synthesis. Doping, co-doping and modification of TiO2 samples with nitrogen, sulfur and platinum increased their photocatalytic activity up to 6 times.