2005
DOI: 10.1016/j.compscitech.2004.09.010
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Constitutive modelling of viscoelastic unloading of short glass fibre-reinforced polyethylene

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Cited by 27 publications
(11 citation statements)
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“…On the other hand, they usually involve numerous material parameters (especially in case of anisotropy), the identification of which being possibly tricky and fastidious. This approach has thus not been very applied to SGFR polymers, and works regarding the use of phenomenological models for this kind of material are often limited to random orientation of the short fibers [20][21][22][23]. However, [24] have proposed a phenomenological viscoelastic-viscoplastic model for the nonlinear response, in which the viscoplastic flow is formulated according to the fiber orientation tensor.…”
Section: Cyclic Behavior: Scale Transition Methods or Macroscopic Modementioning
confidence: 97%
“…On the other hand, they usually involve numerous material parameters (especially in case of anisotropy), the identification of which being possibly tricky and fastidious. This approach has thus not been very applied to SGFR polymers, and works regarding the use of phenomenological models for this kind of material are often limited to random orientation of the short fibers [20][21][22][23]. However, [24] have proposed a phenomenological viscoelastic-viscoplastic model for the nonlinear response, in which the viscoplastic flow is formulated according to the fiber orientation tensor.…”
Section: Cyclic Behavior: Scale Transition Methods or Macroscopic Modementioning
confidence: 97%
“…In the past decade, the time-and rate-dependent responses of polyethylenes at ambient conditions, as well as at elevated temperatures have been studied in a number of publications, see Zhang and Moore (1997), Nitta and Suzuki (1999), Beijer and Spoormaker (2000), Djokovic et al (2000), Pegoretti et al (2000), Mano et al (2001), van Dommelen et al (2003), Dasari and Misra (2003), Bergstrom et al (2004), Hong et al (2004), Remond (2005), Mrabet et al (2005), Nikolov et al (2006), Colak and Dusunceli (2006), Elleuch and Taktak (2006), Christiansen (2007a,b), andBen Hadj Hamouda et al (2007), to mention a few. Although several variants of constitutive equations have been proposed for the viscoelastic and viscoplastic behavior of semi-crystalline polymers that reveal an acceptable agreement with observations, these models share common shortcomings: (i) they disregard thermally-induced evolution of microstructure of HDPE in the vicinity of a-relaxation point (in the interval of temperatures between 60 and 80°C), and (ii) their application to fitting observations results in rather high values of the apparent activation energy of solid polyethylene (in the interval between 100 and 200 kJ/mol) which substantially exceed those for polyethylene melts [20-30 kJ/mol (Bin Wadud and Baird, 2000)] and are close to the activation energies for thermal degradation of high-density polyethylene [ranging between 200 and 300 kJ/ mol (Sinfronio et al, 2005;Marazzato et al, 2007)].…”
Section: Introductionmentioning
confidence: 99%
“…Application of the hardening concept to modeling the mechanical response of polymers was initiated by Krempl and his group (Ho and Krempl, 2002;Krempl and Khan, 2003), but fitting of a loadingretraction curve (one cycle only) on polyphenylene oxide by a model with 12 adjustable parameters revealed rather poor agreement with experimental data and an additional improvement of the model was necessary (Colak, 2005). For a comparison of several versions of models with isotropic and kinematic hardening and a discussion of their ability to fit data on polyethylene reinforced with short glass fibers, see Remond (2005).…”
Section: Introductionmentioning
confidence: 98%