Sheet molding compound (SMC) composite has been studied under humid-aging conditions. Diffusion of water within the material, as measured by gravimetry, was found to be in good agreement with the "Langmuir-type" diffusion model developed by Carter and Kibler. In their theory, Carter and Kibler consider the existence of two types of water molecules in the material, «mobile» and «bound». In this study, these two types have been considered separately. Furthermore, Infrared spectroscopy (FTIR) analysis has been performed by decomposition of signals to study the fraction of free (mobile) and hydrogen-bounded water. Thermal analysis and microscopic observations were put forward to explain the two types of water molecules. In this contribution, we found a "bi-phasic" water diffusion. We suggest that the «mobile» water corresponding to the diffusion in the micro-porosities follows a Fickien kinetic, which turns to sigmoidal one at a specific time of immersion τ. Whereas the kinetic of «bound» water, referring to crosslinking and plasticization, follows a sigmoidal kinetic, which turns to Fickien behavior when the overall network is saturated.
In this study, the distributions of both molecular orientation and crystallinity along the flow direction as well as across the thickness direction of injection‐molded specimens of poly(ethylene terephthalate) (PET) molded at different mold temperatures were investigated. The degree of molecular orientation at the surface of the specimens was compared with that of other injected materials (polystyrene, high density polyethylene, liquid crystal polymer) showing different thermal, rheological, and crystallization characteristics. It was found that the molecular orientation at the skin layer of the molding increases with the polymer relaxation time, the rigidity of the polymer molecules, and the crystallization rate of the polymer. Moreover, in the case of PET, it was found that the crystallinity at the skin layer and in the core of the molding depends on the mold temperature. For low mold temperatures, near the gate, the maximum of crystallinity was observed at the subskin layer because of the “shear‐induced crystallization” generated during the filling stage. On increasing the mold temperature, the maximum of crystallinity was found to shift to the skin layer as a result of the decrease of the thickness of this layer. For low mold temperatures, the variation of the molecular orientation in the thickness direction was found to be much the same as for the crystallinity of the polymer. This result indicates that the shear‐induced crystallization process improves the degree of molecular orientation in the flow direction since it inhibits the relaxation process of the polymer molecules.
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