Zinc oxide arouses considerable interest since it has many applications—in microelectronics, environmental decontaminations, biomedicine, photocatalysis, corrosion, etc. The present investigation describes the green synthesis of nanosized ZnO particles using a low-cost, ecologically friendly approach compared to the classical methods, which are aimed at limiting their harmful effects on the environment. In this study, ZnO nanoparticles were prepared using an extract of Mentha arvensis (MA) leaves as a stabilizing/reducing agent, followed by hydrothermal treatment at 180 °C. The resulting powder samples were characterized by X-ray diffraction (XRD) phase analysis, infrared spectroscopy (IRS), scanning electron microscopy (SEM), and electron paramagnetic resonance (EPR). The specific surface area and pore size distribution were measured by the Brunauer–Emmett–Taylor (BET) method. Electronic paramagnetic resonance spectra were recorded at room temperature and at 123 K by a JEOL JES-FA 100 EPR spectrometer. The intensity of the bands within the range of 400–1700 cm⁻¹ for biosynthesized ZnO (BS-Zn) powders decreased with the increase in the Mentha arvensis extract concentration. Upon increasing the plant extract concentration, the relative proportion of mesopores in the BS-Zn samples also increased. It was established that the photocatalytic performance of the biosynthesized powders was dependent on the MA concentration in the precursor solution. According to EPR and PL analyses, it was proved that there was a presence of singly ionized oxygen vacancies (V₀⁺) and zinc interstitials (Zn_i). The use of the plant extract led to changes in the morphology, phase composition, and structure of the ZnO particles, which were responsible for the increased photocatalytic rate of discoloration of Malachite Green dye.

This study aimed to present the differences in the corrosion properties and protective ability of two bi-layer systems obtained on low-carbon steel in a model corrosive medium of 5% NaCl solution. These newly developed systems consist of Zn-Co (3 wt.%) or Zn-Ni (10 wt.%) alloy coatings as under-layers and a very thin TiO₂ sol-gel film as a top-layer. Scanning electron microscopy (SEM) is used for characterization of the surface morphology of the samples indicating that some quantitative differences appear as a result of the different composition of both zinc alloys. Surface topography is investigated by means of atomic force microscopy (AFM), and the hydrophobic properties are studied by contact angle (CA) measurements. These investigations demonstrate that both sample types possess grain nanometric surface morphology and that the contact angle decreases very slightly. X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) are used for characterization of the chemical composition and electronic structure of the samples. The roughness R_q of the Zn-Ni/TiO₂ is 49.5 nm, while for Zn-Co/TiO₂, the R_q value is 53.4 nm. The water contact angels are 93.2 and 95.5 for the Zn-Ni/TiO₂ and Zn-Co/TiO₂ systems, respectively. These investigations also show that the co-deposition of Zn and Ni forms a coating consisting entirely of Ni₂Zn₁₁, while the other alloy contains Zn, Co and the intermetallic compound CoZn₁₃. The corrosion resistance and protective ability are estimated by potentiodynamic polarization (PDP) curves, as well as polarization resistance (R_p) measurements for a prolonged test period (35 days). The results obtained are compared with the corrosion characteristics of ordinary zinc coating with an equal thickness. The experimental data presents the positive influence of the newly developed systems on the enhanced protective properties of low-carbon steel in a test environment causing a localized corrosion—lower corrosion current density of about one magnitude of order (~10⁻⁶ A.cm⁻² for both systems and ~10⁻⁵ A.cm⁻² for Zn) and an enhanced protective ability after 35 days (~10,000–17,000 ohms for the systems and ~900 ohms for Zn).

Novel fibrous cellulosic substrates impregnated with meta-polybenzimidazole (PBI)-stabilized carbon nanotubes/zinc oxide with different weight content of ZnO and with the use of dimethylacetamide as dispersant media. The pristine ZnO nanoparticle powder was prepared by plant extract-mediated synthesis using Vaccinium vitis-idaea L. The green synthesized ZnO possesses an average crystallite size of 15 nm. The formation of agglomerates from ZnO NPs with size 250 nm–350 nm in the m-PBI@CNTs/ZnO was determined. The prepared materials were investigated by PXRD analysis, XPS, SEM, EDS, AFM, and TEM in order to establish the phase and surface composition, structure, and morphology of the hybrids. The potential of the synthesized hybrid composites to degrade methylene blue (MB) dye as a model contaminant in aqueous solutions under UV illumination was studied. The photocatalytic results show that in the course of the photocatalytic reaction, the m-PBI@CNTs/ZnO 1:3 photocatalyst leads to the highest degree of degradation of the methylene blue dye (67%) in comparison with the other two studied m-PBI@CNTs/ZnO 1:1 and 1:2 composites (48% and 41%). The antibacterial activity of ZnO nanoparticles and the hybrid CNT materials was evaluated by the RMDA and the dynamic contact method, respectively. The profound antibacterial effect of the m-PBI@CNTs/ZnO hybrids was monitored for 120 h of exposition in dark and UV illumination regimes. The photocatalytic property of ZnO nanoparticles significantly shortens the time for bactericidal action of the composites in both regimes. The m-PBI@CNTs/ZnO 1:2 combination achieved complete elimination of 5.10⁵ CFU/mL E. coli cells after 10 min of UV irradiation.

This work presents the enhanced corrosion resistance of newly developed two-layer composite coatings deposited on low-carbon steel: electrodeposited zinc alloy coatings (Zn–Ni with 10 wt.% Ni (ZN) or Zn–Co with 3 wt.% Co (ZC), respectively) and a top ZrO₂ sol–gel layer. Surface morphology peculiarities and anti-corrosion characteristics were examined using scanning electron microscopy (SEM), energy dispersive spectroscopy (EDX), atomic force microscopy (AFM), water contact angle (WCA) measurements, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) analyses, potentiodynamic polarization (PDP) curves, corrosion potential (Ecorr), polarization resistance (Rp) measurements (for a prolonged period of 25 days) and open-circuit potential (OCP). The results were compared with the corrosion peculiarities of usual zinc coating. The zirconia top coatings in both systems were amorphous and dense, possessing hydrophobic nature. The experimental data revealed an increased corrosion resistance and protective ability of the ZC system in comparison to that of ZN due to its smooth, homogeneous surface and the presence of poorly crystallized oxides (ZnO and Co₃O₄), both later playing the role of a barrier for corrosive agents.