Glass fibers: Quo vadis?

[no abstract available

Polyolefine Composites Reinforced by Rice Husk and Saw Dust

Due to the global demand for fibrous light-weight materials, research on composites reinforced with plant materials has increased. Natural fiber reinforced composites offer several advantages: light weight, competitive specific mechanical properties, easy processing, large volume availability, low cost, and low environmental footprint. Especially, using agricultural wastes such as rice husk, saw dust etc. as fillers/fibres in composites provides the chance to improve material properties while improving their sustainability. In the present work, rice husk and saw dust were chosen as fillers for their differing morphology, aspect ratios, and difference of structure. As matrices, polyethylene (PE) and polypropylene (PP) were studied, either neat or modified with maleic anhydride grafted PP/PE as coupling agent or compatibilizer between hydrophobic matrices and hydrophilic bio-fillers. The bending modulus is improved due to filler addition. In presence of compatibilizer, the improved interfacial interaction leads to improved bending and tensile strength as well as toughness. Furthermore, the influence of the filler and compatibilizer on composite properties such as hardness, dynamic mechanical behaviour, thermal expansion, thermal degradation, melting and crystallisation behaviour are presented

Beschleunigte Alterung von Glasfasern in alkalischen Lösungen: Einflüsse auf die mechanischen Eigenschaften

In alkalischen Lösungen führt die Reaktion von Hydroxylionen mit den Si-O-Si-Bindungen des Glasnetzwerks zur Bildung hydratisierter Oberflächen und gelöstem Silikat. Der Grad der Korrosion bzw. der Alterung der Glasfaser ist abhängig von der chemischen Zusammensetzung des Glases und Korrosionslösung sowie von Zeit und Temperatur. Die Untersuchung von Glasfasern verschiedener chemischer Zusammensetzung in NaOH- sowie Zementlösungen zeigte, dass die inhibierende Wirkung von Ca-Ionen zu einem veränderten Korrosionsmechanismus führt. Dies konnte anhand der mechanischen Eigenschaften der Glasfasern sowie rasterelektronenmikroskopischen Untersuchungen gezeigt werden. Während die Korrosion in NaOH-Lösung zu einer ausgeprägten Umwandlung der gesamten äußeren Glasfaserschicht in Reaktionsprodukte führte, zeigten Glasfasern in Zementlösung bei gleichem pH-Wert einen stark lokal begrenzten, punktförmigen Angriff. Daraus resultieren unterschiedliche mechanische Eigenschaften der Glasfasern in Abhängigkeit von der gewählten Korrosionslösung

CVD-Grown CNTs on Basalt Fiber Surfaces for Multifunctional Composite Interphases

Chemical vapor deposition (CVD) is used as a method for the synthesis of carbon nanotubes (CNT) on substrates, most commonly pre-treated by a metal-catalyst. In this work, the capability of basalt fiber surfaces was investigated in order to stimulate catalyst-free growth of carbon nanotubes. We have carried out CVD experiments on unsized, sized, and NaOH-treated basalt fibers modified by growth temperature and a process gas mixture. Subsequently, we investigated the fiber surfaces by SEM, AFM, XPS and carried out single fiber tensile tests. Growth temperatures of 700 °C as well as 800 °C may induce CNT growth, but depending on the basalt fiber surface, the growth process was differently affected. The XPS results suggest surficial iron is not crucial for the CNT growth. We demonstrate that the formation of a corrosion shell is able to support CNT networks. However, our investigations do not expose distinctively the mechanisms by which unsized basalt fibers sometimes induce vertically aligned CNT carpets, isotropically arranged CNTs or no CNT growth. Considering data from the literature and our AFM results, it is assumed that the nano-roughness of surfaces could be a critical parameter for CNT growth. These findings will motivate the design of future experiments to discover the role of surface roughness as well as surface defects on the formation of hierarchical interphases

Cure Kinetics of Epoxy Nanocomposites Affected by MWCNTs Functionalization: A Review

The current paper provides an overview to emphasize the role of functionalization of multiwalled carbon nanotubes (MWCNTs) in manipulating cure kinetics of epoxy nanocomposites, which itself determines ultimate properties of the resulting compound. In this regard, the most commonly used functionalization schemes, that is, carboxylation and amidation, are thoroughly surveyed to highlight the role of functionalized nanotubes in controlling the rate of autocatalytic and vitrification kinetics. The current literature elucidates that the mechanism of curing in epoxy/MWCNTs nanocomposites remains almost unaffected by the functionalization of carbon nanotubes. On the other hand, early stage facilitation of autocatalytic reactions in the presence of MWCNTs bearing amine groups has been addressed by several researchers. When carboxylated nanotubes were used to modify MWCNTs, the rate of such reactions diminished as a consequence of heterogeneous dispersion within the epoxy matrix. At later stages of curing, however, the prolonged vitrification was seen to be dominant. Thus, the type of functional groups covalently located on the surface of MWCNTs directly affects the degree of polymer-nanotube interaction followed by enhancement of curing reaction. Our survey demonstrated that most widespread efforts ever made to represent multifarious surface-treated MWCNTs have not been directed towards preparation of epoxy nanocomposites, but they could result in property synergism

Coating of Carbon Nanotube Fibers: Variation of Tensile Properties, Failure Behavior, and Adhesion Strength

An experimental study of the tensile properties of CNT fibers and their interphasial behavior in epoxy matrices is reported. One of the most promising applications of CNT fibers is their use as reinforcement in multifunctional composites. For this purpose, an increase of the tensile strength of the CNT fibers in unidirectional composites as well as strong interfacial adhesion strength is desirable. However, the mechanical performance of the CNT fiber composites manufactured so far is comparable to that of commercial fiber composites. The interfacial properties of CNT fiber/polymer composites have rarely been investigated and provided CNT fiber/epoxy interfacial shear strength (IFSS) of 14.4 MPa studied by the microbond test. In order to improve the mechanical performance of the CNT fibers, an epoxy compatible coating with nano-dispersed aqueous-based polymeric film formers and low viscous epoxy resin, respectively, was applied. For impregnation of high homogeneity, low molecular weight epoxy film formers and polyurethane film formers were used. The aqueous-based epoxy film formers were not crosslinked and able to interdiffuse with the matrix resin after impregnation. Due to good wetting of the individual CNT fibers by the film formers, the degree of activation of the fibers was improved, leading to increased tensile strength and Young’s modulus. Cyclic tensile loading and simultaneous determination of electric resistance enabled to characterize the fiber’s durability in terms of elastic recovery and hysteresis. The pull-out tests and SEM study reveal different interfacial failure mechanisms in CNT fiber/epoxy systems for untreated and film former treated fibers, on the one hand, and epoxy resin treated ones, on the other hand. The epoxy resin penetrated between the CNT bundles in the reference or film former coated fiber, forming a relatively thick CNT/epoxy composite layer and thus shifting the fracture zone within the fiber. In contrast to this, shear sliding along the interface between the matrix and the outer fiber layer impregnated with the resin was observed for epoxy resin-coated fibers. These fibers have been successfully pulled out of the matrix droplets and shown that the average local interfacial shear stress value was 63 MPa (with apparent IFSS values 33–60 MPa). The interfacial frictional stress between the fiber and the matrix was rather high (9.5 MPa), which can be attributed to the complex structure of the interface and the fiber twisting

Glass Fibers: Quo Vadis?

Since the early 1930s, the process of melting glass and subsequently forming fibers, in particular discontinuous fiber glass or continuous glass filaments, evolved into commercial-scale manufacturing.[...

Investigation of Transcrystalline Interphases in Polypropylene/Glass Fiber Composites Using Micromechanical Tests

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

Commingled Yarn Spinning for Thermoplastic/Glass Fiber Composites

Online commingled yarns were spun with three different polymeric matrices, namely polypropylene (PP), polyamide (PA) and polylactic acid (PLA) and glass fibers. Tailored sizings were applied for the three matrices and the resulting mechanical performance of unidirectional composites was evaluated and compared. Significant improvements in the fiber/matrix bonding were achieved by employed sizing chemistry in order to achieve multifunctional interphases. The pure silane coupling agents provide the best performance for all matrices investigated. However, an additional film former has to be added in order to achieve fiber processing. Film formers compatible to the matrices investigated were adapted. The consolidation behavior during isothermal molding was investigated for polypropylene matrix. Different fiber volume contents could be realized and the resulting mechanical properties were tested