Abstract

Fiber reinforced thermoplastic composites have shown to be attractive for industry as they can be reused, reshaped, welded and repaired, while keeping mechanical properties on par with thermoset composites. Since thermoplastics usually have high melt viscosities unsuitable for liquid composite molding processes, in-situ synthesis of PA6 from ε-caprolactam is considered. Its reactive mix has low viscosity which allows impregnation. However, the coupled crystallization and polymerization affects the resin viscosity and its flow is altered by the dual-scale permeability of the fiber preform. Thus, to predict the local differences in the thermoplastics properties, a coupled polymerization crystallization model needs to be integrated in the LCM processing simulation at representative scales. This study aims to propose a reliable simulation of the resin flow through a fibrous preform. Hence, viscosity measurements on the reactive mix are achieved using a rheometer with parallel-plate geometry, aiming to associate a viscosity model with the Hillier coupled polymerization-crystallization model previously determined by Vicard. The full chemorheological model will then be integrated into a simulation of LCM process in OpenFOAM®, an open source CFD software in order to follow the extent of the synthesis in the resin flow during the process. As a future work, simulations including microscale tow information extracted from a real textile specimen will permit to investigate the effect of permeability and double scale porosity in fibrous preforms on the final polymerization rate and crystallinity.

Highlights

  • Fiber reinforced thermoplastic composites have garnered interest as they can have mechanical properties comparable with thermoset composite while allowing additional possibilities in part fabrication such as welding or reshaping

  • As the reactive mix for polyamide 6 (PA6) is based on the ε-caprolactam monomer, it has very high fluidity adapted to liquid composite molding processes (LCM) with fast in-situ polymerization of the thermoplastic matrix [1]

  • The front is tracked using the volume of fluid (VOF) method (4) with an interface compression term where vc is the relative velocity between the two phases [10]

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Summary

Introduction

Fiber reinforced thermoplastic composites have garnered interest as they can have mechanical properties comparable with thermoset composite while allowing additional possibilities in part fabrication such as welding or reshaping. Vicard et al [5] used differential scanning calorimetry (DSC) to gather experimental data on a reactive mix with suitable synthesis duration for LCM processes. This has highlighted the different synthesis characteristics with relation to temperature and allowed the identification of a modified Hillier coupling of polymerization and crystallization model. A preliminary modelling procedure to simulate the flow of the reactive mix is presented It integrates the polymerization kinetics from Vicard et al [5] and the rheokinetics proposed by Davé et al [6].

Reactive mix
Rheological measurement setup
Isothermal rheology at 453 K
Temperature dependence of the reactive mix
PA6 flow modelling
Computational method
Preliminary simulation of the reactive mix injection
Conclusion
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