“…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)].…”