Iskanje po repozitoriju

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Opis: The contamination of water bodies by microorganisms is seen as a highly significant issue that poses a threat to human and animal well-being. The primary objective of this master thesis is to develop and evaluate an environmentally friendly photoelectrochemical (PEC) method using porous Fe₂O₃ thin films for the disinfection of wastewater. This thesis presents the novel application of porous Fe₂O₃ thin films, which were produced using a cost-effective spin-coating technique, to improve the process of PEC disinfection. The PEC approach has been demonstrated to be highly effective in disinfection of wastewaters deliberately contaminated with E. coli bacteria. The crystallinity of the Fe₂O₃ porous thin films was confirmed using X-ray diffraction (XRD), while the film morphology was studied using scanning electron microscopy (SEM). The PEC disinfection procedures were conducted in the presence of two separate electrolytes, sodium sulfite (Na₂SO₃) and sodium chloride (NaCl), which were chosen for their specific roles in improving the effectiveness of disinfection. The PEC method shown efficacy in inactivating E. coli, with 45% of the bacteria being inactivated in the presence of 2 mM Na₂SO₃ and complete inactivation achieved with 20 mM NaCl. The findings suggest that the PEC disinfection process is a highly efficient and eco-friendly technology that can be used as a practical substitute for traditional disinfection methods. As a result, it has potential applications in ensuring public safety and safeguarding the environment, particularly in relation to wastewater treatment.
Ključne besede: Treated wastewater, Disinfection, Escherichia coli, Photoelectrochemical oxidation, Fe2O3 thin films, Sodium sulfite and Sodium chloride.
Objavljeno v RUNG: 09.09.2024; Ogledov: 776; Prenosov: 13
Celotno besedilo (2,23 MB)

Opis: A γ-alumina support functionalized with transition metals is one of the most widely used industrial catalysts for the total oxidation of volatile organic compounds (VOCs) as air pollutants at higher temperatures (280−450 °C). By rational design of a bimetal CuFe-γ-alumina catalyst, synthesized from a dawsonite alumina precursor, the activity in total oxidation of toluene as a model VOC at a lower temperature (200−380 °C) is achieved. A fundamental understanding of the catalyst and the reaction mechanism is elucidated by advanced microscopic and spectroscopic characterizations as well as by temperature-programmed surface techniques. The nature of the metal−support bonding and the optimal abundance between Cu−O−Al and Fe−O−Al species in the catalysts leads to synergistic catalytic activity promoted by small amounts of iron (Fe/Al = 0.005). The change in the metal oxide−cluster alumina interface is related to the nature of the surfaces to which the Cu atoms attach. In the most active catalyst, the CuO6 octahedra are attached to 4 Al atoms, while in the less active catalyst, they are attached to only 3 Al atoms. The oxidation of toluene occurs via the Langmuir−Hinshelwood mechanism. The presented material introduces a prospective family of low-cost and scalable oxidation catalysts with superior efficiency at lower temperatures.
Ključne besede: Iron oxide clusters, copper oxide clusters, alumina support, synergistic effect, low-temperature total catalytic oxidation, toluene, Cu, Fe XANES, EXAFS
Objavljeno v RUNG: 06.07.2023; Ogledov: 2705; Prenosov: 27
Celotno besedilo (11,05 MB)
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Opis: Strategies to generate high-valence metal species capable of oxidizing water often employ composition and coordination tuning of oxide-based catalysts, where strong covalent interactions with metal sites are crucial. However, it remains unexplored whether a relatively weak “non-bonding” interaction between ligands and oxides can mediate the electronic states of metal sites in oxides. Here we present an unusual non-covalent phenanthroline-CoO2 interaction that substantially elevates the population of Co4+ sites for improved water oxidation. We find that phenanthroline only coordinates with Co2+ forming soluble Co(phenanthroline)2(OH)2 complex in alkaline electrolytes, which can be deposited as amorphous CoOxHy film containing non-bonding phenanthroline upon oxidation of Co2+ to Co3+/4+. This in situ deposited catalyst demonstrates a low overpotential of 216 mV at 10 mA cm−2 and sustainable activity over 1600 h with Faradaic efficiency above 97%. Density functional theory calculations reveal that the presence of phenanthroline can stabilize CoO2 through the non-covalent interaction and generate polaron-like electronic states at the Co-Co center.
Ključne besede: water oxidation, cobalt hydroxide, ligand-metal interactions
Objavljeno v RUNG: 23.02.2023; Ogledov: 2654; Prenosov: 19
Celotno besedilo (1,77 MB)

Opis: The development of affordable, low-iridium-loading, scalable, active, and stable catalysts for the oxygen-evolution reaction (OER) is a requirement for the commercialization of proton-exchange membrane water electrolyzers (PEMWEs). However, the synthesis of high-performance OER catalysts with minimal use of the rare and expensive element Ir is very challenging and requires the identification of electrically conductive and stable high-surface-area support materials. We developed a synthesis procedure for the production of large quantities of a nanocomposite powder containing titanium oxynitride (TiONx) and Ir. The catalysts were synthesized with an anodic oxidation process followed by detachment, milling, thermal treatment, and the deposition of Ir nanoparticles. The anodization time was varied to grow three different types of nanotubular structures exhibiting different lengths and wall thicknesses and thus a variety of properties. A comparison of milled samples with different degrees of nanotubular clustering and morphology retention, but with identical chemical compositions and Ir nanoparticle size distributions and dispersions, revealed that the nanotubular support morphology is the determining factor governing the catalyst’s OER activity and stability. Our study is supported by various state-of-the-art materials’ characterization techniques, like X-ray photoelectron spectroscopy, scanning and transmission electron microscopies, Xray powder diffraction and absorption spectroscopy, and electrochemical cyclic voltammetry. Anodic oxidation proved to be a very suitable way to produce high-surface-area powder-type catalysts as the produced material greatly outperformed the IrO2 benchmarks as well as the Ir-supported samples on morphologically different TiONx from previous studies. The highest activity was achieved for the sample prepared with 3 h of anodization, which had the most appropriate morphology for the effective removal of oxygen bubbles.
Ključne besede: electrocatalysis, oxygen-evolution reaction, TiONx-Ir powder catalyst, iridium nanoparticles, anodic oxidation, morphology−activity correlation
Objavljeno v RUNG: 04.01.2021; Ogledov: 3409; Prenosov: 0
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Ključne besede: Wine, reductive aroma, oxidation, good practice, Slovenia
Objavljeno v RUNG: 19.09.2018; Ogledov: 4867; Prenosov: 22
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