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Publisher: Basel : MDPI × Subject: Interface ×

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Now showing 1 - 3 of 3
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    Polymeric Coatings for AR-Glass Fibers in Cement-Based Matrices: Effect of Nanoclay on the Fiber-Matrix Interaction
    (Basel : MDPI, 2021) Bompadre, Francesca; Scheffler, Christina; Utech, Toni; Donnini, Jacopo
    Polymeric coatings are widely used to enhance the load bearing capacity and chemical durability of alkali-resistant glass (AR-glass) textile in cement-based composites. The contact zone between coated yarns and concrete matrix plays a major role to enable the stress transfer and has still to be improved for the full exploitation of the mechanical behavior of the composite. As a new approach, this paper studies how the addition of nanoclay particles in the polymer coating formulation can increase the chemical bond between organic coating and inorganic matrix. This includes the description of the water-based coating preparation by dispersing sodium montmorillonites, whereby the resulting coating nanostructure is characterized by X-ray diffraction and energy dispersive X-ray spectroscopy. Single glass fibers were treated by dip-coating. Atomic force microscopy was used to determine the surface roughness, and the effect on the fiber tensile properties was studied. Moreover, the morphological and chemical characteristics of the coatings were compared with the results obtained from single fiber pull-out (SFPO) tests. It was shown that the incorporation of nanoclays leads to increased interfacial shear strength arising from the ability of nanoclay particles to nucleate hydration products in the fiber-matrix contact zone.
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    Investigation of transcrystalline interphases in polypropylene/glass fiber composites using micromechanical tests
    (Basel : MDPI, 2018) Brodowsky, Hanna; Mäder, Edith
    In composites, a strong interphase between the components is essential for mechanical properties. By using a suitable sizing (i.e., surface modification) of the fiber, the interphase may be varied, e.g., by suppressing or promoting heterogeneous nucleation of a thermoplastic matrix. In the latter case, three-dimensional transcrystallized interphases with properties differing from those of the bulk matrix are formed. Polypropylene-glass fiber composites are prepared as single-fiber model composites with (a) sizings either inducing or suppressing a transcrystalline interphase, (b) different amounts of modifier maleic acid anhydride grafted polypropylene, and (c) different molecular weights of the matrix polymer. These are studied in quasi-static or cyclic load tests. Static tests permit insights in the interfacial characteristics such as critical interface energy release rate, adhesion strength and frictional stress. Cyclic tests on these model composites can be used to study the nature of dissipative processes and the damage behavior. Atomic Force Microscopy (AFM) investigations of the fiber fracture surfaces provide supplementary information. The transcrystalline layer can indeed improve the mechanical parameters (a 70–100% increase of strength and a 25 or 125% increase in toughness, depending on the molecular weight (MW) of the matrix polymer at low modifier concentration). However, the effect is partially neutralized by an opposing effect: high nucleation in the bulk in samples with commonly used concentrations of modifier.
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    Influence of Polycation Composition on Electrochemical Film Formation
    (Basel : MDPI, 2018) Schneider, Sabine; Janssen, Corinna; Klindtworth, Elisabeth; Mergel, Olga; Möller, Martin; Plamper, Felix
    The effect of polyelectrolyte composition on the electrodeposition onto platinum is investigated using a counterion switching approach. Film formation of preformed polyelectrolytes is triggered by oxidation of hexacyanoferrates(II) (ferrocyanide), leading to polyelectrolyte complexes, which are physically crosslinked by hexacyanoferrate(III) (ferricyanide) ions due to preferential ferricyanide/polycation interactions. In this study, the electrodeposition of three different linear polyelectrolytes, namely quaternized poly[2-(dimethylamino)ethyl methacrylate] (i.e., poly{[2-(methacryloyloxy)ethyl]trimethylammonium chloride}; PMOTAC), quaternized poly[2-(dimethylamino)ethyl acrylate] (i.e., poly{[2-(acryloyloxy)ethyl]trimethylammonium chloride}; POTAC), quaternized poly[N-(3-dimethylaminopropyl)methacrylamide] (i.e., poly{[3-(methacrylamido)propyl]trimethylammonium chloride}; PMAPTAC) and different statistical copolymers of these polyelectrolytes with N-(3-aminopropyl)methacrylamide (APMA), are studied. Hydrodynamic voltammetry utilizing a rotating ring disk electrode (RRDE) shows the highest deposition efficiency DE for PMOTAC over PMAPTAC and over POTAC. Increasing incorporation of APMA weakens the preferred interaction of the quaternized units with the hexacyanoferrate(III) ions. At a sufficient APMA content, electrodeposition can thus be prevented. Additional electrochemical quartz crystal microbalance measurements reveal the formation of rigid polyelectrolyte films being highly crosslinked by the hexacyanoferrate(III) ions. Results indicate a different degree of water incorporation into these polyelectrolyte films. Hence, by adjusting the polycation composition, film properties can be tuned, while different chemistries can be incorporated into these electrodeposited thin hydrogel films.