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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. [ABSTRACT FROM AUTHOR]

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. [ABSTRACT FROM AUTHOR]

Monitoring water content and predicting the water-induced drop in strength of fiber-reinforced composites are of great importance for the oil and gas and marine industries. Fourier transform infrared (FTIR) spectroscopic methods are broadly available and often used for process and quality control in industrial applications. A benefit of using such spectroscopic methods over the conventional gravimetric analysis is the possibility to deduce the mass of an absolutely dry material and subsequently the true water content, which is an important indicator of water content-dependent properties. The objective of this study is to develop an efficient and detailed method for estimating the water content in epoxy resins and fiber-reinforced composites. In this study, Fourier transform near-infrared (FT-NIR) spectroscopy was applied to measure the water content of amine-epoxy neat resin. The method was developed and successfully extended to glass fiber-reinforced composite materials. Based on extensive measurements of neat resin and composite samples of varying water content and thickness, regression was performed, and the quantitative absorbance dependence on water content in the material was established. The mass of an absolutely dry resin was identified, and the true water content was obtained. The method was related to the Beer–Lambert law and explained in such terms. A detailed spectroscopic method for measuring water content in resins and fiber-reinforced composites was developed and described. [ABSTRACT FROM AUTHOR]

This study examines the diffusion of water in fiber-reinforced polymer (FRP) laminated composites, comprising epoxy resin and unidirectional glass fibers, at different material and structural scales. Experiments on the diffusion of neat resin, FRP laminas in the axial and transverse fiber directions, FRP laminated composites with different stacking sequences, and FRP plates, rods, and pipes are conducted to obtain the diffusion processes at different length scales. Simultaneously, a diffusion model for a laminated composite is formulated to mathematically describe the multi-axial diffusion processes in FRP composites at various length scales, i.e., single lamina, laminated stacking sequence, and component. The study shows that the diffusivity constants calibrated from neat epoxy resin and unidirectional laminas are adequate to predict the diffusion responses of laminated composite systems and structural components of larger sizes. This capability is useful in predicting the long-term diffusion responses of FRP composites of complex geometries and large sizes where conducting diffusion tests on such systems is not feasible. [ABSTRACT FROM AUTHOR]