The contamination of both soil and water by nitrobenzene (NB) is a problem that has been studied, where several reactive agents have been developed for the degradation of this compound as well as different methods. Nanoparticles with semiconductive properties have been studied for organic compounds photodegradation due to their assistance in optimizing the degradation processes. Two of the most promising photocatalysts are ZnO and TiO₂ because of their optimal results. In the present work the performance of the zinc peroxide (ZnO₂) nanoparticles was evaluated. ZnO₂ nanoparticles were synthesized from zinc acetate and hydrogen peroxide using the Sol-Gel method under ultrasound assistance. The characterization was carried out by UV–Vis spectroscopy, infrared Fourier transform total reflectance (ATR-FT-IR) spectroscopy, Raman spectroscopy, X-ray diffraction (XRD), Zeta potential, dynamic light scattering (DLS), field emission scanning electron microscopy (FE-SEM), and Energy Dispersive X-ray spectroscopy (EDX). The experiments for the degradation of NB were carried out in a photoreactor with UV lamps of 254 nm at 25 °C, using a solution of nitrobenzene with the nanoparticles. The best conditions for NB photodegradation were 30 ppm (ZnO₂) and 15 ppm (NB) at pH 2, reaching up to 90% degradation in 2 h. The intermediates formed during the photodegradation of NB were identified by gas chromatography mass spectrometry.

In the present work, chemically modified graphene oxide (GO) was incorporated as a crosslinking agent into thin-film composite (TFC) nanofiltration (NF) membranes for water desalination applications, which were prepared by the interfacial polymerization (IP) method, where the monomers were piperazine (PIP) and trimesoyl chloride (TMC). GO was functionalized with monomer-containing groups to promote covalent interactions with the polymeric film. The composite GO/polyamide (PA) was prepared by incorporating amine and acyl chloride groups into the structure of GO and then adding these chemical modified nanomaterial during IP. The effect of functionalized GO on membrane properties and performance was investigated. Chemical composition and surface morphology of the prepared GO and membranes were analyzed by thermogravimetric analysis (TGA), Raman spectroscopy, FTIR spectroscopy, X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), scanning electron microscopy (SEM), atomic force microscopy (AFM), and transmission electron microscopy (TEM). The fabricated composite membranes exhibited a significant increase in permeance (from 1.12 to 1.93 L m⁻² h⁻¹ bar⁻¹) and salt rejection for Na₂SO₄ (from 95.9 to 98.9%) and NaCl (from 46.2 to 61.7%) at 2000 ppm, when compared to non-modified membranes. The amine- and acyl chloride-functionalized GO showed improved dispersibility in the respective phase.

A Gamma irradiation and photochemical crosslinking/grafting of poly(2-hydroxyethyl methacrylate) (PHEMA) and poly(2-hydroxyethyl methacrylate-co-poly(ethylene glycol) methacrylate) (poly(HEMA-co-PEGMA)) hydrogels onto polyethyleneterephtalate fabric (PET) surfaces were evaluated, in order to obtain a hydrophilic homogeneous coating onto PET fabrics. The materials were characterized by FTIR-ATR, SEM, EDS, and thermal analysis. Furthermore, silver nanoparticles (AgNPs) were loaded by in situ reduction of AgNO₃, and its antibacterial activity against Staphylococcus aureus and Escherichia coli was determined. Results showed a ticker coating of hydrogel using gamma radiation and stronger in deep modification of the fibers; however, by the photochemical method, a thin coating with good coverage of PET surface was obtained. The differences in hydrophilicity, thermal properties, and antibacterial activity of the coated fabrics by using both methods were rather small.

The effect of the nature of the catalyst on the performance and mechanism of the hydrogen oxidation reaction (HOR) is discussed for the first time in this work. HOR is an anodic reaction that takes place in anionic exchange membrane fuel cells (AEMFCs) and hydrogen pumps (HPs). Among the investigated catalysts, Pt exhibited the best performance in the HOR. However, the cost and the availability limit the usage. Co is incorporated as a co-catalyst due to its oxophylic nature. Five different PtCo catalysts with different Pt loading values were synthesized in order to decrease Pt loading. The catalytic activities and the reaction mechanism were studied via electrochemical techniques, and it was found that both features are a function of Pt loading; low-Pt-loading catalysts (Pt loading < 2.7%) led to a high half-wave potential in the hydrogen oxidation reaction, which is related to higher activation energy and an intermediate Tafel slope value, related to a mixed HOR mechanism. However, catalysts with moderate Pt loading (Pt loading > 3.1%) exhibited lower E_1/2 than the other catalysts and exhibited a mechanism similar to that of commercial Pt catalysts. Our results demonstrate that Co plays an active role in the HOR, facilitating H_ads desorption, which is the rate-determining step (RDS) in the mechanism of the HOR.