A reverse-micelle sol–gel method was chosen for the preparation of Fe-doped TiO₂ samples that were employed in the photodegradation of the crystal violet dye under visible light irradiation in a batch reactor. The dopant amount was varied to assess the optimal photocatalyst composition towards the target dye degradation. The photocatalysts were characterized through a multi-technique approach, envisaging XRPD and QPA as obtained by Rietveld refinement, FE-SEM analysis, DR UV−vis spectroscopy, N₂ adsorption/desorption isotherms measurement at −196 °C, ζ-potential measurement, and XPS analysis. The physical-chemical characterization showed that the adopted synthesis method allows obtaining NPs with uniform shape and size and promotes the introduction of Fe into the titania matrix, finally affecting the relative amounts of the three occurring polymorphs of TiO₂ (anatase, rutile and brookite). By increasing the Fe content, the band gap energy decreases from 3.13 eV (with undoped TiO₂) to 2.65 eV (with both 2.5 and 3.5 wt.% nominal Fe contents). At higher Fe content, surface Fe oxo-hydroxide species occur, as shown by DR UV-vis and XP spectroscopies. All the Fe-doped TiO₂ photocatalysts were active in the degradation and mineralization of the target dye, showing a TOC removal higher than the undoped sample. The photoactivity under visible light was ascribed both to the band-gap reduction (as confirmed by phenol photodegradation) and to dye sensitization of the photocatalyst surface (as confirmed by photocatalytic tests carried out using different visible-emission spectra LEDs). The main reactive species involved in the dye degradation were determined to be positive holes.

Phenol is an important chemical compound since it is a precursor of the industrial production of many materials and useful compounds. Nowadays, phenol is industrially produced from benzene by the multi-step “cumene process”, which is energy consuming due to high temperature and high pressure. Moreover, in the “cumene process”, the highly explosive cumene hydroperoxide is produced as an intermediate. To overcome these disadvantages, it would be useful to develop green alternatives for the synthesis of phenol that are more efficient and environmentally benign. In this regard, great interest is devoted to processes in which the one-step oxidation of benzene to phenol is achieved, thanks to the use of suitable catalysts and oxidant species. This review article discusses the direct oxidation of benzene to phenol in the liquid phase using different catalyst formulations, including homogeneous and heterogeneous catalysts and photocatalysts, and focuses on the reaction mechanisms involved in the selective conversion of benzene to phenol in the liquid phase.

In this study, a highly polluted wastewater from tannery industry is treated by photocatalysis using home-made N-doped TiO ₂ as catalyst. The doping by nitrogen of titania particles leads to a reduction in the absorption threshold from 3.2 to 2.5 eV, permitting the absorption of radiation characterized by a wavelength in the visible spectrum.Experiments were carried out by using different light sources, in particular white LEDs, blue LEDs, and UV lamps, with the aim to evaluate the process efficiency at different operating conditions. The obtained performances were compared with those using an undoped commercial TiO ₂ catalyst (Degussa P25).Moreover, a simplified mathematical model capable to correlate the power input of the used light sources, the geometrical properties of the reactor, and emitting sources spectra with the performances of the photocatalytic reaction was developed.