Photocatalytic UV-Induced Approach for Discoloration of Bromocresol Purple, Bromothymol Blue Dyes and Their Mixture Using Nix Fe3−xO4/Fe2O3/AC Composites

The nickel ferrite-activated carbon samples NiFe2O4/Activated carbon and NixFe3−xO4/Fe2O3/AC, x = 0.25; 0.5 obtained by co-precipitation followed by thermal treatment in inert atmosphere, were studied for discoloration of Bromocresol Purple (BCP), Bromothymol Blue (BTB) dyes and their mixture as model contaminants under UV-A light. The prepared materials were investigated by XPS, PXRD and XRF analysis, FT-IR spectroscopy, SEM, EDX, BET method and TG analysis. The photocatalyst with composition NixFe3−xO4-AC, x = 1 has demonstrated the highest photocatalytic activity towards discoloration of the BTB in comparison with the others tested materials NixFe3−xO4/Fe2O3/AC, x = 0.25; 0.5. These results can be explained with the smaller particle sizes, the mesoporous structure, the higher degree of crystallinity and higher content of hydroxyl groups. This study proved that the obtained nickel ferrite-activated carbon materials are suitable as photocatalysts for discoloration of the BTB dye. They have demonstrated also relatively high adsorption ability towards BCP dye

Surface and Morphological Features of ZrO2 Sol-Gel Coatings Obtained by Polymer Modified Solution

Thin, homogeneous ZrO2 films were obtained by spin coating method from ZrOCl2 8H2O solution, modified with polyethylene glycol (PEG) (Mw = 400). The films have thickness of 80 nm and refractive index of about 1.45, which varied with the amount of added PEG. The thermal behaviour of the precursor was studied with thermogravimetry and differential thermal analysis (TG-DTA). The X-ray diffraction (XRD) analysis revealed the presence of a mixture of monoclinic and tetragonal ZrO2 polycrystalline phases with nanosized crystallites. The formation of hydrogen bonds among the organic and inorganic components was proved by means of Fourier transform infrared spectroscopy (FT-IR) analysis, while the different defect centres were investigated with electron paramagnetic resonance (EPR) spectroscopy. The scanning electron microscopy (SEM) images showed that the samples are dense and crack-free, with ganglia-like nanostructure. It was established that the addition of polymer resulted in the introduction of free volume in the films, which also varied with the content of PEG in the precursor solution

Electrocatalysts Based on Novel Carbon Forms for the Oxidation of Sulphite

Described herewith is an electrochemical method to decontaminate sulphur compounds. Studies were carried out of sulphites (SO32−) oxidation on a range of anode catalysts. The electrocatalysts were characterized by scanning electron microscopy, XRD, XPS and BET. Polarization curves were recorded of electrodes incorporating lyophilized higher fullerenes and manganese oxides. The experiments showed that lyophilized higher fullerenes and C60/C70 fullerene catalysts in conjunction with manganese oxides electrochemically convert sulphites (SO32−) to sulphates (SO42−). The oxidation products do not poison the electrodes. The XPS analysis shows that the catalysts incorporating DWCNTs, MWCNTs and higher fullerenes have a higher concentration of sp3C carbon bonding leading to higher catalytic activity. It is ascertained that higher fullerenes play a major role in the synthesis of more effective catalysts. The electrodes built by incorporating lyophilized catalysts containing higher fullerenes and manganese oxides are shown as most promising in the effective electrochemical decontamination of industrial and natural wastewaters

Electrocatalysts Based on Novel Carbon Forms for the Oxidation of Sulphite

Described herewith is an electrochemical method to decontaminate sulphur compounds. Studies were carried out of sulphites (SO32−) oxidation on a range of anode catalysts. The electrocatalysts were characterized by scanning electron microscopy, XRD, XPS and BET. Polarization curves were recorded of electrodes incorporating lyophilized higher fullerenes and manganese oxides. The experiments showed that lyophilized higher fullerenes and C60/C70 fullerene catalysts in conjunction with manganese oxides electrochemically convert sulphites (SO32−) to sulphates (SO42−). The oxidation products do not poison the electrodes. The XPS analysis shows that the catalysts incorporating DWCNTs, MWCNTs and higher fullerenes have a higher concentration of sp3C carbon bonding leading to higher catalytic activity. It is ascertained that higher fullerenes play a major role in the synthesis of more effective catalysts. The electrodes built by incorporating lyophilized catalysts containing higher fullerenes and manganese oxides are shown as most promising in the effective electrochemical decontamination of industrial and natural wastewaters

Protective Characteristics of TiO₂ Sol-Gel Layer Deposited on Zn-Ni or Zn-Co Substrates

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 Rq of the Zn-Ni/TiO2 is 49.5 nm, while for Zn-Co/TiO2, the Rq 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 (Rp) 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)

Modified Approach Using Mentha arvensis in the Synthesis of ZnO Nanoparticles—Textural, Structural, and Photocatalytic Properties

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 (Zni). 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