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Now showing 1 - 9 of 9
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    Fe3O4 Nanoparticles Grown on Cellulose/GO Hydrogels as Advanced Catalytic Materials for the Heterogeneous Fenton-like Reaction
    (Washington, DC : ACS Publications, 2019) Chen, Yian; Pötschke, Petra; Pionteck, Jürgen; Voit, Brigitte; Qi, Haisong
    Cellulose/graphene oxide (GO)/iron oxide (Fe3O4) composites were prepared by coprecipitating iron salts onto cellulose/GO hydrogels in a basic solution. X-ray photoelectron spectroscopy (XPS), Fourier-transform infrared, and X-ray diffraction characterization showed that Fe3O4 was successfully coated on GO sheets and cellulose. Cellulose/GO/Fe3O4 composites showed excellent catalytic activity by maintaining almost 98% of the removal of acid orange 7 (AO7) and showed stability over 20 consecutive cycles. This performance is attributable to the synergistic effect of Fe3O4 and GO during the heterogeneous Fenton-like reaction. Especially, the cellulose/GO/Fe3O4 composites preserve their activity by keeping the ratio of Fe3+/Fe2+ at 2 even after 20 catalysis cycles, which is supported by XPS analysis.
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    Synthesis of Modified Poly(vinyl Alcohol)s and Their Degradation Using an Enzymatic Cascade
    (Weinheim : Wiley-VCH, 2023) von Haugwitz, Gerlis; Donnelly, Kian; Di Filippo, Mara; Breite, Daniel; Phippard, Max; Schulze, Agnes; Wei, Ren; Baumann, Marcus; Bornscheuer, Uwe T.
    Poly(vinyl alcohol) (PVA) is a water-soluble synthetic vinyl polymer with remarkable physical properties including thermostability and viscosity. Its biodegradability, however, is low even though a large amount of PVA is released into the environment. Established physical-chemical degradation methods for PVA have several disadvantages such as high price, low efficiency, and secondary pollution. Biodegradation of PVA by microorganisms is slow and frequently involves pyrroloquinoline quinone (PQQ)-dependent enzymes, making it expensive due to the costly cofactor and hence unattractive for industrial applications. In this study, we present a modified PVA film with improved properties as well as a PQQ-independent novel enzymatic cascade for the degradation of modified and unmodified PVA. The cascade consists of four steps catalyzed by three enzymes with in situ cofactor recycling technology making this cascade suitable for industrial applications.
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    Degradation Behavior of Silk Nanoparticles - Enzyme Responsiveness
    (Washington, DC : ACS Publ., 2018) Wongpinyochit, Thidarat; Johnston, Blair F.; Seib, F. Philipp
    Silk nanoparticles are viewed as promising vectors for intracellular drug delivery as they can be taken up into cells by endocytosis and trafficked to lysosomes, where lysosomal enzymes and the low pH trigger payload release. However, the subsequent degradation of the silk nanoparticles themselves still requires study. Here, we report the responsiveness of native and PEGylated silk nanoparticles to degradation following exposure to proteolytic enzymes (protease XIV and α-chymotrypsin) and papain, a cysteine protease. Both native and PEGylated silk nanoparticles showed similar degradation behavior over a 20 day exposure period (degradation rate: protease XIV > papain ≫ α-chymotrypsin). Within 1 day, the silk nanoparticles were rapidly degraded by protease XIV, resulting in a ∼50% mass loss, an increase in particle size, and a reduction in the amorphous content of the silk secondary structure. By contrast, 10 days of papain treatment was necessary to observe any significant change in nanoparticle properties, and α-chymotrypsin treatment had no effect on silk nanoparticle characteristics over the 20-day study period. Silk nanoparticles were also exposed ex vivo to mammalian lysosomal enzyme preparations to mimic the complex lysosomal microenvironment. Preliminary results indicated a 45% reduction in the silk nanoparticle size over a 5-day exposure. Overall, the results demonstrate that silk nanoparticles undergo enzymatic degradation, but the extent and kinetics are enzyme-specific.
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    Determination of the Entire Stent Surface Area by a New Analytical Method
    (Basel : MDPI, 2020) Saqib, Muhammad; Bernhardt, Ricardo; Kästner, Markus; Beshchasna, Natalia; Cuniberti, Gianaurelio; Opitz, Jörg
    Stenting is a widely used treatment procedure for coronary artery disease around the world. Stents have a complex geometry, which makes the characterization of their corrosion difficult due to the absence of a mathematical model to calculate the entire stent surface area (ESSA). Therefore, corrosion experiments with stents are mostly based on qualitative analysis. Additionally, the quantitative analysis of corrosion is conducted with simpler samples made of stent material instead of stents, in most cases. At present, several methods are available to calculate the stent outer surface area (SOSA), whereas no model exists for the calculation of the ESSA. This paper presents a novel mathematical model for the calculation of the ESSA using the SOSA as one of the main parameters. The ESSA of seven magnesium alloy stents (MeKo Laser Material Processing GmbH, Sarstedt, Germany) were calculated using the developed model. The calculated SOSA and ESSA for all stents are 33.34%(±0.26%) and 111.86 mm (±0.85 mm), respectively. The model is validated by micro-computed tomography (micro-CT), with a difference of 12.34% (±0.46%). The value of corrosion rates calculated using the ESSA computed with the developed model will be 12.34% (±0.46%) less than that of using ESSA obtained by micro-CT.
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    Photocatalytic degradation and toxicity evaluation of diclofenac by nanotubular titanium dioxide–PES membrane in a static and continuous setup
    (London : RSC Publishing, 2015) Fischer, K.; Kühnert, M.; Gläser, R.; Schulze, A.
    Diclofenac is a commonly used anti-inflammatory drug, which has been found in surface waters. Advanced oxidation processes (AOPs) seem to be the most suitable technique to prevent the entry of diclofenac and other pollutants into surface waters. TiO2 is especially reliable in mineralizing many organic molecules. The combination of TiO2 nanotubes with a polymer microfiltration membrane (polyethersulfone, PES) showed high photocatalytic activity by degrading diclofenac combined with an excellent membrane performance and long-term stability. By continuously degrading pollutants from water via a cross-flow setup, the molecules to be degraded are transported right to the membrane surface so that the overall reaction rate is increased. The toxicity of diclofenac was reduced by photocatalysis and photolysis; however, photocatalysis had greater impact. Moreover, the complete degradation of pollutants is very important to avoid highly toxic intermediate products.
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    Sonication-assisted liquid phase exfoliation of two-dimensional CrTe3 under inert conditions
    (Amsterdam [u.a.] : Elsevier Science, 2023) Synnatschke, Kevin; Moses Badlyan, Narine; Wrzesińska, Angelika; Lozano Onrubia, Guillermo; Hansen, Anna–Lena; Wolff, Stefan; Tornatzky, Hans; Bensch, Wolfgang; Vaynzof, Yana; Maultzsch, Janina; Backes, Claudia
    Liquid phase exfoliation (LPE) has been used for the successful fabrication of nanosheets from a large number of van der Waals materials. While this allows to study fundamental changes of material properties’ associated with reduced dimensions, it also changes the chemistry of many materials due to a significant increase of the effective surface area, often accompanied with enhanced reactivity and accelerated oxidation. To prevent material decomposition, LPE and processing in inert atmosphere have been developed, which enables the preparation of pristine nanomaterials, and to systematically study compositional changes over time for different storage conditions. Here, we demonstrate the inert exfoliation of the oxidation-sensitive van der Waals crystal, CrTe3. The pristine nanomaterial was purified and size-selected by centrifugation, nanosheet dimensions in the fractions quantified by atomic force microscopy and studied by Raman, X-ray photoelectron spectroscopy (XPS), energy-dispersive X-ray spectroscopy (EDX) and photo spectroscopic measurements. We find a dependence of the relative intensities of the CrTe3 Raman modes on the propagation direction of the incident light, which prevents a correlation of the Raman spectral profile to the nanosheet dimensions. XPS and EDX reveal that the contribution of surface oxides to the spectra is reduced after exfoliation compared to the bulk material. Further, the decomposition mechanism of the nanosheets was studied by time-dependent extinction measurements after water titration experiments to initially dry solvents, which suggest that water plays a significant role in the material decomposition.
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    Degradation of glyphosate in water by the application of surface corona discharges
    (Bristol : IWA Publishing, 2021) Zocher, Katja; Gros, Peter; Werneburg, Matthias; Brüser, Volker; Kolb, Juergen F.; Leinweber, Peter
    Glyphosate (GLP) is one of the most widely applied herbicides, and is found ubiquitously in the environment. The removal of glyphosate from waste water and soil is challenging and can be achieved with chemical or biological methods, which, nevertheless, suffer from different disadvantages. The application of a physical plasma for the removal of GLP in water was examined by the application of surface corona discharges in a wire-to-cylinder setup filled with argon. The plasma was ignited at the liquid surface without any additives. By applying a photometric method, GLP was detected after derivatisation with fluorenyl methoxycarbonyl chloride, whereas phosphate was determined with ammonium molybdate. A GLP degradation rate of 90.8% could be achieved within a treatment time of 30 minutes with an estimated energy efficiency of 0.32 g/kWh.
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    Design of Polymer-Embedded Heterogeneous Fenton Catalysts for the Conversion of Organic Trace Compounds
    (Basel : MDPI, 2021) Horn, Christoph; Ihmann, Stephanie; Müller, Felix; Pospiech, Doris; Borchert, Konstantin B. L.; Hommel, Rolf; Qin, Kaite; Licha, Kai; Allertz, Peter J.; Drache, Marco
    Advanced oxidation processes are the main way to remove persistent organic trace compounds from water. For these processes, heterogeneous Fenton catalysts with low iron leaching and high catalytic activity are required. Here, the preparation of such catalysts consisting of silica-supported iron oxide (Fe2O3/SiOx) embedded in thermoplastic polymers is presented. The iron oxide catalysts are prepared by a facile sol–gel procedure followed by thermal annealing (calcination). These materials are mixed in a melt compounding process with modified polypropylenes to stabilize the Fe2O3 catalytic centers and to further reduce the iron leaching. The catalytic activity of the composites is analyzed by means of the Reactive Black 5 (RB5) assay, as well as by the conversion of phenol which is used as an example of an organic trace compound. It is demonstrated that embedding of silica-supported iron oxide in modified polypropylene turns the reaction order from pseudo-first order (found for Fe2O3/SiOx catalysts), which represents a mainly homogeneous Fenton reaction, to pseudo-zeroth order in the polymer composites, indicating a mainly heterogeneous, surface-diffusion-controlled process.
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    Verbundprojekt: Batterie – Stationär in Sachsen (BaSta), Teilvorhaben: Leibniz IFW : Schlussbericht ; Berichtszeitraum: 01.11.2012-30.04.2016
    (Hannover : Technische Informationsbibliothek (TIB), 2016) Eckert, Jürgen; Giebeler, Lars
    Die Entwicklung und Umsetzung umfasst eines völlig neuartigen Batteriekonzeptes, der die Vorteile der bisherigen Na-S-Hochtemperaturbatterien (z.B. niedrige Kosten und hohe Verfügbarkeit der notwendigen Rohstoffe) mit der Performance moderner Lithium-Ionenbatterien, jedoch auf Na-Ionenbasis, im Niedertemperaturbereich verknüpft. Dazu müssen neue Elektroden- bzw. Separatormaterialien mit vorteilhafter Interaktion und Degradationsstabilität in verschiedenen neuartigen Elektrolyten entwickelt werden. Darüber hinaus werden geeignete Verfahren zur Herstellung und Fertigung dieser Komponenten zu Niedertemperatur-Na-S-Batterien generiert. Die Ziele sollen durch die außerordentlich enge Vernetzung mehrerer Professuren der TU Dresden mit verschiedenen Instituten der Fraunhofer Gesellschaft, dem Leibniz IFW Dresden e.V. und der TU Bergakademie Freiberg erreicht werden. Der Arbeitsplan sieht eine 'bottom up' Strategie von der Materialentwicklung und Charakterisierung über die Werkstoffprozessierung hin zur Systementwicklung und -charakterisierung vor. Die universitären Einrichtungen arbeiten dabei vorwiegend grundlagenorientiert auf dem Gebiet der Materialentwicklung für einen völlig neuen Batterietyp. Die dabei gewonnenen Erkenntnisse werden unmittelbar in die anwendungsorientierte Forschung überführt. Entscheidend ist die interaktive Zusammenarbeit zu allen Zeitpunkten und auf allen Ebenen des Gesamtvorhabens.