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STRUCTURAL PROPERTIES OF MANGANESE-FUNCTIONALIZED SILICA AEROGELS : MASTER'S THESIS
Tatjana Kobal, 2016, magistrsko delo

Opis: Manganese-functionalized silica with interparticle mesoporosity and isolated Mn sites (Mn/Si = 0.01) is an excellent Fenton catalyst for water cleaning. However, there is a problem that needs to be solved, i.e., Mn leaching from the silica support during the reaction. The solution may lie in using aerogels as the silicate supports for the manganese. The goal of this master thesis is the synthesis and characterization of manganese-functionalized silica aerogels with different Mn/Si molar ratios and a determination of their structural properties. The emphasis is on the preparation of manganese-functionalized silica aerogels with isolated manganese sites. Firstly, manganese-functionalized microporous and mesoporous silicates with a molar ratio Mn/Si = 0.005–0.02 were synthesized according to the literature and characterized as reference materials for manganese-functionalized aerogels. Manganese silicalite-1 (MnS-1) as a microporous zeolite-type silicate and manganese-functionalized silica (MnKIL-2) as a mesoporous silicate were prepared by the sol-gel process with a hydrothermal and solvothermal treatment, respectively. MnS-1 and MnKIL-2 with a molar ratio of Mn/Si ≤ 0.01 contain manganese as isolated sites in the silica framework and with a molar ratio of Mn/Si > 0.01 contain manganese as manganese oxides. Secondly, manganese-functionalized aerogels (MnAEG) with a molar ratio Mn/Si = 0.005–0.02, were prepared according to the acid-base of the sol-gel polymerization of a tetraethylorthosilicate precursor, which is followed in combination with a supercritical drying using CO2. The prepared materials were characterized using the following techniques: X-ray powder diffraction (XRD), energy-dispersive X-ray elemental analysis (EDX), nitrogen physisorption, scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The characterization results on manganese-functionalized aerogels (MnAEG) showed Mn oxide nanoparticles incorporated into the aerogel already at a low Mn concentration (Mn/Si = 0.005), which means that Mn aerogels are not promising silica supports for Mn catalysts applied for water cleaning, because they do not contain isolated Mn sites.
Ključne besede: : SiO2 aerogels, manganese-functionalized SiO2 aerogels, sol–gel process, CO2 supercritical drying
Objavljeno v RUNG: 02.09.2016; Ogledov: 5783; Prenosov: 239
.pdf Celotno besedilo (4,37 MB)

3.
ORR stability of Mn–Co/polypyrrole nanocomposite electrocatalysts studied by quasi in-situ identical-location photoelectron microspectroscopy
Patrizia Bocchetta, Belen Aleman, Matteo Amati, Mattia Fanetti, Andrea Goldoni, Luca Gregoratti, Maya Kiskinova, Claudio Mele, Hikmet Sezen, Benedetto Bozzini, 2016, izvirni znanstveni članek

Opis: The stability of pyrolyzed Mn–Co/polypyrrole (PPy) nanocomposites towards the Oxygen Reduction Reaction (ORR) in alkaline solution, was studied with a close-knit group of complementary microscopic and space-resolved spectroscopic approaches: Atomic Force Microscopy (AFM), Scanning and High-Resolution Transmission Electron Microscopy (SEM, HRTEM) and identical-location Scanning PhotoElectron Microscopy (SPEM). Tracking quasi-in situ the morphochemical evolution of the Mn–Co/PPy catalyst upon electrochemical aging under ORR conditions by this multi-technique approach, has allowed to clarify the key physico-chemical processes underlying the dramatic impact of Co additions to stability improvement.
Ključne besede: Mixed manganese oxides, Polypyrrole, Oxygen reduction, Electrocatalysis, Nanocomposites, X-ray photoelectron microspectroscopy
Objavljeno v RUNG: 25.07.2016; Ogledov: 5149; Prenosov: 0
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4.
Photocatalytic Activity of Zirconium- and Manganese- Codoped Titania in Aqueous Media: The Role of the Metal Dopant and its Incorporation Site
O. L. Pliekhov, Iztok Arčon, Nataša Novak Tušar, Urška Lavrenčič Štangar, 2016, izvirni znanstveni članek

Opis: The development of efficient TiO2-based photocatalysts for water treatment is mainly performed by doping with transition metals or by establishing junctions between different phases, metal–semiconductor or semiconductor–semiconductor. We present, for the first time, the synthesis of Zr- and Mn-modified TiO2 by a redesigned sol–gel technique that allows the formation of heterometallic bridges on the TiO2 surface. Cations of the doping metals are located in the pores of mesoporous anatase and attached to the crystalline TiO2 walls. The presence of the Zr enhances the photoactivity of the TiO2 catalyst. However, the introduction of Mn decreases the photocatalytic efficiency in a nonadditive manner. The inhibition effect was assigned to the side reaction between hydroxyl radicals and Mn ions. The fact that Mn effectively scavenges the hydroxyl radicals and, consequently, inhibits the whole oxidation process is direct proof that hydroxyl radicals are the main reactive species in the photocatalytic oxidative processes on TiO2 surfaces in aqueous media and the process of COH generation is the rate-determining step, which was confirmed using a method based on the decolorization of a commercial dye Bezaktiv Blau in a reaction with Fenton’s reagent as a source of hydroxyl radicals.
Ključne besede: doping, manganese, oxidation, X-ray absorption spectroscopy, zirconium
Objavljeno v RUNG: 21.07.2016; Ogledov: 4105; Prenosov: 0
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5.
Removal of manganese in batch and fluidized bed systems using beads of zeolite a as adsorbent
Mina Jovanovic, Iztok Arčon, Janez Kovač, Nataša Novak Tušar, Bojana Obradovic, Nevenka Rajić, 2016, izvirni znanstveni članek

Opis: In this study the uptake capacity of Mn(II) ions by zeolite A beads was investigated for different initial Mn concentration (100e400 mg Mn dm^-3) in batch mode at 25e55 C. The obtained adsorption capacity varying from 30 to 50 mg Mn g^-1 demonstrated a high affinity of zeolite A towards Mn(II) present in solutions. Kinetic studies indicated the intra-particle diffusion as the rate limiting step up to 45 C with apparent diffusivities in the range (1.2e2.0) x 10^-13 m2 s^-1 and the activation energy of 21.9 kJ mol^-1, which implies strong interactions between the zeolite A and Mn ions. At 55 C ion-exchange became the rate limiting step. The adsorption isotherms were studied at 25 C showing that the Mn adsorption is the best described by the Langmuir model suggesting a homogenous zeolite surface. XPS analysis of the Mnloaded beads showed that there is no surface accumulation of Mn but an almost uniform Mn distribution inside zeolite A, whereas XANES and EXAFS suggested that the adsorption of Mn(II) was followed by the Mn(II) oxidation and oxide formation. Regeneration of the spent zeolite was examined in 8 adsorption/desorption cycles by a chelating Na2EDTA in a fluidized column. It has been found that zeolite A beads could be reused for at least 4 cycles with satisfactory Mn(II) adsorption efficiencies of about 70%.
Ključne besede: Zeolite A Manganese Adsorption kinetics EXAFS/XANES XPS
Objavljeno v RUNG: 01.04.2016; Ogledov: 5178; Prenosov: 0
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