Recently, significant events took place that added immensely to the sociotechnical pressure for developing sustainable composite recycling solutions, namely (1) a ban on composite landfilling in Germany in 2009, (2) the first major wave of composite wind turbines reaching their End-of-Life (EoL) and being decommissioned in 2019–2020, (3) the acceleration of aircraft decommissioning due to the COVID-19 pandemic, and (4) the increase of composites in mass production cars, thanks to the development of high volume technologies based on thermoplastic composites. Such sociotechnical pressure will only grow in the upcoming decade of 2020s as other countries are to follow Germany by limiting and banning landfill options, and by the ever-growing number of expired composites EoL waste. The recycling of fiber reinforced composite materials will therefore play an important role in the future, in particular for the wind energy, but also for aerospace, automotive, construction and marine sectors to reduce environmental impacts and to meet the demand. The scope of this manuscript is a clear and condensed yet full state-of-the-art overview of the available recycling technologies for fiber reinforced composites of both low and high Technology Readiness Levels (TRL). TRL is a framework that has been used in many variations across industries to provide a measurement of technology maturity from idea generation (basic principles) to commercialization. In other words, this work should be treated as a technology review providing guidelines for the sustainable development of the industry that will benefit the society. The authors propose that one of the key aspects for the development of sustainable recycling technology is to identify the optimal recycling methods for different types of fiber reinforced composites. Why is that the case can be answered with a simple price comparison of E-glass fibers (~2 $/kg) versus a typical carbon fiber on the market (~20 $/kg)—which of the two is more valuable to recover? However, the answer is more complicated than that—the glass fiber constitutes about 90% of the modern reinforcement market, and it is clear that different technologies are needed. Therefore, this work aims to provide clear guidelines for economically and environmentally sustainable End-of-Life (EoL) solutions and development of the fiber reinforced composite material recycling.
Glass fibres slowly degrade due to dissolution when exposed to water. Such environmental aging results in the deterioration of the mechanical properties. In structural offshore and marine applications, as well as in the wind energy sector, R-glass fibre composites are continuously exposed to water and humid environments for decades, with a typical design lifetime being around 25 years or more. During this lifetime, these materials are affected by various temperatures, acidity levels, and mechanical loads. A Dissolving Cylinder Zero-Order Kinetic (DCZOK) model was able to explain the long-term dissolution of R-glass fibres, considering the influence of the pH, temperature, and stress corrosion. The effects of these environmental conditions on the dissolution rate constants and activation energies of dissolution were obtained. Experimentally, dissolution was measured using High Resolution Inductively Coupled Plasma Mass Spectrometry (HR-ICP-MS). For stress corrosion, a custom rig was designed and used. The temperature showed an Arrhenius-type influence on the kinetics, increasing the rate of dissolution exponentially with increasing temperature. In comparison with neutral conditions, basic and acidic aqueous environments showed an increase in the dissolution rates, affecting the lifetime of glass fibres negatively. External loads also increased glass dissolution rates due to stress corrosion. The model was able to capture all of these effects.
Service lifetimes of polymers and polymer composites are impacted by environmental ageing. The validation of new composites and their environmental durability involves costly testing programs, thus calling for more affordable and safe alternatives, and modelling is seen as such an alternative. The state-of-the-art models are systematized in this work. The review offers a comprehensive overview of the modular and multiscale modelling approaches. These approaches provide means to predict the environmental ageing and degradation of polymers and polymer composites. Furthermore, the systematization of methods and models presented herein leads to a deeper and reliable understanding of the physical and chemical principles of environmental ageing. As a result, it provides better confidence in the modelling methods for predicting the environmental durability of polymeric materials and fibre-reinforced composites.
Fluid diffusion in fiber reinforced composites is typically anisotropic. Diffusivity in the fiber direction is faster than in the transverse direction. The reason for this behavior is not yet fully understood. In this work, dealing with glass fiber epoxy composite immersed in distilled water, an experimental procedure for determination of anisotropic diffusion constants from a laminate is presented. The method has the advantage that it does not require sealing of the samples edges because 3-D anisotropic diffusion theory is implemented for obtaining the diffusion constants. A microscale model is presented, where matrix and fiber bundles are modeled separately. The matrix properties have been obtained experimentally and the fiber bundle properties have been deduced by the composite homogenized diffusivity model. The analysis indicates that the anisotropic diffusion of the composite is due to inherent anisotropic properties of the fiber bundles.
Understanding the strength degradation of glass and carbon fibers due to exposure to liquids over time is important for structural applications. A model has been developed for glass fibers that links the strength reduction in water to the increase of the Griffith flaw size of the fibers. The speed of the increase is determined by regular chemical dissolution kinetics of glass in water. Crack growth and strength reduction can be predicted for several water temperatures and pH, based on the corresponding dissolution constants. Agreement with experimental results for the case of water at 60 °C with a pH of 5.8 is reasonably good. Carbon fibers in water and toluene and glass fibers in toluene do not chemically react with the liquid. Subsequently no strength degradation is expected and will be confirmed experimentally. All fiber strength measurements are carried out on bundles. The glass fibers are R-glass.
Fiber-reinforced polymers (FRP) are widely used in structural applications. Long-term properties of such materials exposed to water are of high concern and interest, especially for subsea and offshore applications. The objective of this study is to identify the mechanisms and to identify whether drop in properties of diamine-cured mixed DGEBA-HDDGE is reversible upon drying the material to its initial water content. The properties of interest are mechanical strength, elastic properties and fatigue performance, as well as changes in chemical structure. The effect of absorbed water on the properties of the resin is evaluated, and hygrothermal effects and aging mechanisms are discussed. Furthermore, it is shown experimentally that the tension fatigue S-N curve of a wet epoxy resin can be estimated by shifting the S-N curve of a dry material proportionally to a reduction in static tensile strength due to hygrothermal effects.
Long-term creep properties and the effect of water are important for fiber reinforced polymer (FRP) composite materials used in offshore applications. Epoxies are often used as a matrix material in such composites. A typical design lifetime of offshore FRP structures is 25 or more years in direct contact with water leading to some deterioration of the material properties. Knowing and predicting the extent of the material property deterioration in water is of great interest for designers and users of the offshore FRP structures. It has been established that the time–temperature superposition principle (TTSP) is a useful tool for estimating changes in properties of polymer materials at long times or extreme temperatures. In this work, a time–temperature–plasticization superposition principle (TTPSP) is described and used for predicting the long-term creep behavior of an epoxy compound. The studied epoxy does not degrade chemically via hydrolysis or chain scission but is negatively affected by plasticization with water. The methodology enables prediction of the long-term viscoelastic behavior of amorphous polymers at temperatures below the glass transition (Tg) using short-term creep experimental data. The results also indicate that it is possible to estimate the creep behavior of the plasticized polymer based on the short-term creep data of the respective dry material and the difference between Tg values of dry polymer and plasticized polymer. The methodology is useful for accelerated testing and for predicting the time-dependent mechanical properties of a plasticized polymer below the glass transition temperature.
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