Abstract
Under high-temperature creep conditions the dependence of the steady-state creep rate (εs) on applied stress (σ) and temperature (T) can be described by an equation
εs = Ao n exp (−Qc/RT)………(1)
where A and n are constants and Qc the activation energy for creep. For most pure metals n is ∼4.0 and Qc = QSD (activation energy for self-diffusion). Creep theories can readily account for these stress- and temperature-dependences. However, with two-phase alloys n and Qc are generally substantially higher than those for pure metals and single-phase alloys. For example, with T.D. nickel n ≃ 40 and Q c = 795 kJ/lmol compared with n = 5.0 and Q c = 276 for pure nickel. Many precipitation-hardening alloys show the same trends. No creep theories can account for these high n and Q c values. In particular, recovery-creep theories suggest maximum values of n ≃ 4.0 and Q c = Q SD.
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