40 research outputs found

    The behavior of multilayer ceramic protections at quick thermal shock

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    Protective layers of “hot parts” of the turbo engines as well as co-generative systems of energy industry are exposed to a combination of wear factors which may act together at high values.The main goal of the paper is the behavior of some advanced layers, duplex and triplex, multifunctional, ceramics in relation to the most complex wear factor and disturbing as well, the quick thermal shock.The quick thermal shock test installation designed and constructed by the INCAS covers the domain of some high gradients of heating/cooling and is currently integrated in a network of European infrastructure that evaluates the properties of functional layers for turbo engines.Micro-structure inter- and intra- facial changes gradually induced in ceramic structures are highlighted and on this basis their ranking and selection for application on physical parts are established

    The Effect of Clay Type on the Physicochemical Properties of New Hydrogel Clay Nanocomposites

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    This study focuses on the investigation of clay type effect on the final properties of semi-interpenetrated Salecan/poly(methacrylic acid)/clay hydrogel nanocomposites. Previous studies have indicated that the presence of clay in polymer composites leads to better swelling capacity and mechanical properties as functions of clay type. On the other hand, Salecan, which is a water soluble extracellular polysaccharide, was proved to assure greater flexibility to hydrogels. These properties recommend clay and Salecan for semi-interpenetrated hydrogels preparation with specific application in biomedicine. The purpose was to determine the most suitable type of clay as well as Salecan influence for developing the desired water retention/delivery ability and mechanically enhanced semi-interpenetrating polymer network (SIPN) nanocomposites. For our investigations, we have chosen commercially available montmorillonite (ClNa) and different commercial organomodified clay (Cl30B, Cl20A and Cl15A). Several analyses results (FTIR, TGA, DMA, XRD, microscopy and swelling studies) demonstrated that not only the presence of Salecan but also the clay type influenced the structure and properties of the final nanocomposites

    Degradation of keratin substrates by keratinolytic fungi

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    Background: The hydrolysis of keratin wastes by microorganisms is considered a biotechnological alternative for recycling and valorization through keratinolytic microorganisms. Despite their resistant structure, keratin wastes can be efficiently degraded by various microorganisms through the secretion of keratinases,which are promising enzymes for several applications, including detergents, fertilizers, and leather and textile industry. In an attempt to isolate keratinolytic microorganisms that can reach commercial exploitation as keratinase producers, the current work assesses the dynamics of keratin biodegradation by several keratinolytic fungal strains isolated from soil. The activity of fungal strains to degrade keratin substrates was evaluated by SEM, FTRIR-ATR spectra and TGA analysis. Results: SEM observations offered relevant information on interactions between microorganism and structural elements of hair strands. FTIR spectra of the bands at 1035\u20131075 cm-1 assigned to sulfoxide bond appeared because of S\u2013S bond breaking, which demonstrated the initiation of keratin biodegradation. According to TGA, in the second zone of thermal denaturation, where keratin degradation occurs, the highest weight loss of 71.10% was obtained for sample incubated with Fusarium sp. 1A. Conclusions: Among the tested strains, Fusarium sp. 1A was the most active organism in the degradation process with the strongest denaturation of polypeptide chains. Because keratinolytic microorganisms and their enzymes keratinases represent a subject of scientific and economic interest because of their capability to hydrolyze keratin, Fusarium sp. 1A was selected for further studies

    Exploring the Potential of Beneficial <i>Paecilomyces</i> to Improve Plant Growth

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    Introduction: For sustainable agriculture, an attempt has been made to reduce the use of fertilizers and agrochemicals, replacing them instead with biostimulants as viable alternatives [...

    Nanocomposites Based Electrosensitive Platforms for Nitrite and Biogenic Amines Determination

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    Highly electrosensitive platforms have been developed using different nanocomposite materials based on carbon allotropes and different metallic nanoparticles for determination of nitrite and biogenic amines (BAs). The nitrification process occurred in soil represents an important source of pollution. The nitrification consists in biological oxidation of the relatively immobile ammonium (NH4+) to highly mobile nitrate, via nitrite. This process is carried out mainly by the ammonia–oxidizing bacteria (Nitrosomonas sp. and Nitrobacter sp.) present in the soil microbial population [1,2]. The nitrite contamination of ground and surface waters represents the major concern associated with the nitrification process. Additionally, the growing needs for food and environmental safety has led to an increase in research for the detection of biogenic amines (BAs) in recent years. Despite the fact that BAs are increasingly present in food and beverages, causing toxic effects in the body, legislation that limits their presence in food chains needs to be updated, thus requiring sensitive tools for their detection [3,4]. Miniaturized analytical tools have been developed based on nanocomposite materials obtained through combination of different carbon allotrope materials (nanoribbons, nanotubes—single and multiwalled—and nanofibers) with metallic nanoparticles (Ag, Au-Ag, Pt, Cu). Thus, carbon based screen-printed electrodes (SPE) were chemically modified with the obtained nanocomposite materials and further characterized using different electrochemical techniques. In order to allow a selective and sensitive determination of analytes, an electropolymerized film was deposed on the modified sensors. For BAs determination were realized with two configurations of biosensors, a bienzymatic one consisting in immobilization of diamine oxidase (DAO) and horseradish peroxidase (HRP) onto the modified sensors, and, respectively, a mono-enzymatic system based on immobilization of DAO onto the modified sensors. It was taken into account that the charge of carbon-based nanomaterials on the surface of the sensors should not exceed 5%, in order to ensure a low based current. Morpho-structural and electrochemical characterization studies of the modified SPEs have been performed in order to achieve a high sensitivity and selectivity of detection, applying a low overvoltage. The co-polymeric film ensured a better stability of the nanocomposite material layers at the electrode surface and an optimal matrix for enzymes immobilization. Optimization of the nanocomposite-based sensors were performed, and finally detection of biogenic amines was carried out using biosensors based on single-walled carbon nanotubes and Pt nanoparticles, while nitrite determination was performed using multi-walled carbon nanotubes and AgNP modified sensors at applied potentials between −0.45 and +0.6 V vs. Ag/AgCL. The developed sensors and biosensors showed good sensitivities of nitrite and BAs detection. Although the enzyme DAO has a low enough activity to catalyze the oxidation of amine of interest, the detection limits were lowered due to the electrocatalytic activity of nanocomposite materials and the HRP enzyme used

    Synthesis of Zinc Oxide Nanomaterials via Sol-Gel Process with Anti-Corrosive Effect for Cu, Al and Zn Metallic Substrates

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    Nanosized zinc oxide (ZnO) particles modified with different silane coupling agents (octyltriethoxysilane (OTES), octadecyltriethoxysilane (ODTES) and (3-glycidyloxypropyl)trimethoxysilane (GPTMS)) were synthesized in basic catalysis using the sol-gel method. The structure and morphology were characterized by dynamic light scattering (DLS), environmental scanning electron microscopy (ESEM) and Fourier transform infrared spectroscopy (FTIR) for bonding characteristics. The final hybrid materials were deposited on three types of metallic substrates (aluminum (Al), copper (Cu) and zinc (Zn)) in order to obtain coatings with ultrahydrophobic and anti-corrosion properties. Water wettability was studied revealing a contact angle of 145° for the surface covered with ZnO material modified with ODTES. The water contact angle increased with the length of the alkyl chain supplied by the silica precursor. The anti-corrosive behavior of ZnO/silane coupling agents particles deposited on metallic substrates was studied by the linear polarization technique in neutral medium

    Aminopropyl-Silica Hybrid Particles as Supports for Humic Acids Immobilization

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    A series of aminopropyl-functionalized silica nanoparticles were prepared through a basic two step sol-gel process in water. Prior to being aminopropyl-functionalized, silica particles with an average diameter of 549 nm were prepared from tetraethyl orthosilicate (TEOS), using a Stöber method. In a second step, aminopropyl-silica particles were prepared by silanization with 3-aminopropyltriethoxysilane (APTES), added drop by drop to the sol-gel mixture. The synthesized amino-functionalized silica particles are intended to be used as supports for immobilization of humic acids (HA), through electrostatic bonds. Furthermore, by inserting beside APTES, unhydrolysable mono-, di- or trifunctional alkylsilanes (methyltriethoxy silane (MeTES), trimethylethoxysilane (Me3ES), diethoxydimethylsilane (Me2DES) and 1,2-bis(triethoxysilyl)ethane (BETES)) onto silica particles surface, the spacing of the free amino groups was intended in order to facilitate their interaction with HA large molecules. Two sorts of HA were used for evaluating the immobilization capacity of the novel aminosilane supports. The results proved the efficient functionalization of silica nanoparticles with amino groups and showed that the immobilization of the two tested types of humic acid substances was well achieved for all the TEOS/APTES = 20/1 (molar ratio) silica hybrids having or not having the amino functions spaced by alkyl groups. It was shown that the density of aminopropyl functions is low enough at this low APTES fraction and do not require a further spacing by alkyl groups. Moreover, all the hybrids having negative zeta potential values exhibited low interaction with HA molecules
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