6 research outputs found

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

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    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

    Synthesis of Improved Catalytic Materials for High-Temperature Water-gas Shift Reaction

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    In this investigation, we report the preparation and characterization of Co-, Cu- and Mn-substituted iron oxide catalytic materials supported on activated carbon. Co-precipitation method and low temperature treatment were used for their synthesis. The influence of chemical composition, stoichiometry, particle size and dispersity on their catalytic activity was studied. Samples were characterized in all stages of their co-precipitation, heating and spend samples after catalytic tests. The obtained results from room and low temperature Mössbauer spectroscopy were combined with analysis of powder X-ray diffraction patterns (XRD). They revealed the preparation of nano-sized iron oxide materials supported on activated carbon. Relaxation phenomena were registered also for the supported phases. The catalytic performance in the water-gas shift reaction was studied. The activity order was as follows: Cu0.5Fe2.5O4 > Co0.5Fe2.5O4 > Mn0.5Fe2.5O4. Catalytic tests demonstrated very promising results and potential application of studied samples due to their cost-effective composition

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

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    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
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