“…Fig. 7 demonstrates that the apparent activation energy of HDPE far below the melting temperature is about 78 kJ/mol, which is lower than the values provided in some studies grounded on the standard method of superposition of observations in dynamic tests: E a ¼ 110-140 (Zamfirova et al, 2002), E a ¼ 137 (Pegoretti et al, 2000), E a ¼ 150-170 (Mano et al, 2001), E a ¼ 174 (Djokovic et al, 2000), and E a ¼ 207 kJ/mol (Tajvidi et al, 2005), but agrees well with the activation energies E a ¼ 50-140 (Stadler et al, 2005), E a ¼ 65-80 (Boiko et al, 1995), E a ¼ 79-106 (Matsuo et al, 1988), and E a ¼ 89 kJ/mol (Ohta and Yasuda, 1994). The fact that the apparent activation energy of HDPE in the solid state exceeds that of HDPE melt by twice [in the latter case, the activation energy belongs to the interval between 27 and 32 kJ/mol (Bin Wadud and Baird, 2000)] appears to be natural, whereas rather high values of the activation energies (close to the activation energies for thermal degradation of this polymer [E a ¼ 210-270 (Sinfronio et al, 2005) and E a ¼ 260-290 kJ/mol (Marazzato et al, 2007)] ''shows that the physical significance of E a .…”