Cerium oxide (CeO₂) nanoparticles were synthesized with a chemical precipitation method in different experimental conditions using cerium nitrate hexahydrate (Ce(NO₃)₃·6H₂O) as a precursor, modifying the solution pH, the reaction time, and Co atoms as dopants, in order to tune the band gap energy values of the prepared samples. The physical characteristics of the synthesized ceria nanoparticles were evaluated by Fourier transform infrared (FT-IR) spectroscopy, X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), UV–Vis analyses and photoluminescence measurements. XRD data revealed a pure cubic fluorite structure of CeO₂ NPs, the estimation of crystallite sizes by Scherrer’s formula indicates the formation of crystals with dimensions between 11.24 and 21.65 nm. All samples contain nearly spherical CeO₂ nanoparticles, as well as cubic, rhomboidal, triangular, or polyhedral nanoparticles that can be identified by TEM images. The optical investigation of CeO₂ samples revealed that the band gap energy values are between 3.18 eV and 2.85 eV, and, after doping with Co atoms, the E_g of samples decreased to about 2.0 eV. In this study, we managed to obtain CeO₂ NPs with E_g under 3.0 eV by only modifying the synthesis parameters. In addition, by doping with Co ions, the band gap energy value was lowered to 2.0 eV. This aspect leads to promising results that provide an encouraging approach for future photocatalytic investigations.

ZnAlFe_1−xSm_xO₄ (x = 0, 0.02, 0.04, 0.06, 0.08) spinel ferrites were successfully obtained for the first time via a sol–gel autocombustion technique using citric acid as the combustion/chelating agent. These materials were then employed as photocatalysts for the degradation of Evans Blue, considered herein as a model organic pollutant. The XRD and FTIR analysis confirmed the achievement of pure spinel ferrite structures for all the materials. TEM analysis showed that the average particle sizes decline from about 27 for the undoped material to 17 nm for samarium-doped materials, and the magnetic characterization at room temperature indicated the paramagnetic conduct for the studied samples. All the photocatalysts were active in Evans Blue photodegradation. The best photocatalytic performances were observed for the ZnAlFe_0.94Sm_0.06O₄ formulation and explained by the smallest values calculated for lattice parameter, interplanar distance, and particle-size values. By adding H₂O₂ and applying the modelling and optimization of the photocatalytic process for the best material, the half-life of the pollutant decreased significantly from 115 min to about 7 min (about 16-times), and the colour-removal efficiency was almost 100%.

Polymers play a crucial role in multiple industries; however, surface modification is necessary for certain applications. Exposure to non-thermal plasma provides a viable and environmentally beneficial option. Fused deposition molding utilizes biodegradable polylactic acid, although it encounters constraints in biomedical applications as a result of inadequate mechanical characteristics. This study investigates the effects of atmospheric pressure plasma generated by a dielectric barrier discharge system using helium and/or argon on the modification of polylactic acid surfaces, changes in their wettability properties, and alterations in their chemical composition. The plasma source was ignited in either He or Ar and was tailored to fit the best operational conditions for polymer exposure. The results demonstrated the enhanced wettability of the polymer surface following plasma treatment (up to 40% in He and 20% in Ar), with a marginal variation observed among treatments utilizing different gases. The plasma treatments also caused changes in the surface topography, morphology, roughness, and hydrophilicity. Plasma exposure also resulted in observable modifications in the dielectric characteristics, phase transition, and structure. The experimental findings endorse the utilization of plasma technologies at normal air pressure for environmentally friendly processing of polymer materials, specifically for applications that necessitate enhanced adhesion and have carefully selected prerequisites.

6-Iodo-substituted carboxy-quinolines were obtained using a one-pot, three-component method with trifluoroacetic acid as a catalyst under acidic conditions. Iodo-aniline, pyruvic acid and 22 phenyl-substituted aldehydes (we varied the type and number of radicals) or O-heterocycles, resulting in different electronic effects, were the starting components. This approach offers advantages such as rapid response times, cost-effective catalysts, high product yields and efficient purification procedures. A comprehensive investigation was conducted to examine the impact of aldehyde structure on the synthesis pathway. A library of compounds was obtained and characterized by FT-IR, MS, ¹H NMR and ¹³C NMR spectroscopy and single-ray crystal diffractometry. Their antimicrobial activity against S. epidermidis, K. pneumonie and C. parapsilosis was tested in vitro. The effect of iodo-quinoline derivatives on microbial adhesion, the initial stage of microbial biofilm development, was also investigated. This study suggests that carboxy-quinoline derivatives bearing an iodine atom are interesting scaffolds for the development of novel antimicrobial agents.