scholarly journals MCMC inversion of the transient and steady-state creep flow law parameters of dunite under dry and wet conditions

2021 ◽  
Vol 73 (1) ◽  
Author(s):  
Sagar Masuti ◽  
Sylvain Barbot

AbstractThe rheology of the upper mantle impacts a variety of geodynamic processes, including postseismic deformation following great earthquakes and post-glacial rebound. The deformation of upper mantle rocks is controlled by the rheology of olivine, the most abundant upper mantle mineral. The mechanical properties of olivine at steady state are well constrained. However, the physical mechanism underlying transient creep, an evolutionary, hardening phase converging to steady state asymptotically, is still poorly understood. Here, we constrain a constitutive framework that captures transient creep and steady state creep consistently using the mechanical data from laboratory experiments on natural dunites containing at least 94% olivine under both hydrous and anhydrous conditions. The constitutive framework represents a Burgers assembly with a thermally activated nonlinear stress-versus-strain-rate relationship for the dashpots. Work hardening is obtained by the evolution of a state variable that represents internal stress. We determine the flow law parameters for dunites using a Markov chain Monte Carlo method. We find the activation energy $$430\pm 20$$ 430 ± 20   and $$250\pm 10$$ 250 ± 10  kJ/mol for dry and wet conditions, respectively, and the stress exponent $$2.0\pm 0.1$$ 2.0 ± 0.1 for both the dry and wet cases for transient creep, consistently lower than those of steady-state creep, suggesting a separate physical mechanism. For wet dunites in the grain-boundary sliding regime, the grain-size dependence is similar for transient creep and steady-state creep. The lower activation energy of transient creep could be due to a higher jog density of the corresponding soft-slip system. More experimental data are required to estimate the activation volume and water content exponent of transient creep. The constitutive relation used and its associated flow law parameters provide useful constraints for geodynamics applications. Graphical Abstract

1968 ◽  
Vol 3 (4) ◽  
pp. 288-296 ◽  
Author(s):  
D L Marriott

A method has been proposed which approximates transient creep behaviour by the superposition of elastic and steady-state creep deformation. The present paper discusses the errors incurred by this method. It is shown that they are small. Equations are derived which enable corrections to be calculated with moderate accuracy for an important group of creep theories. Some numerical examples are included for comparison.


1988 ◽  
Vol 133 ◽  
Author(s):  
S. E. Hsu ◽  
C. H. Tong ◽  
T. S. Lee ◽  
T. S. Liu

ABSTRACTNi-Al-Cr single crystals with 4 at% Cr and different levels of aluminum content are grown in a directional solidification facility. The crystals are creep tested at temperatures from 760°C to 860°C. Steady state, as well as transient, creep rates are measured. The results show that Cr modified Ni3 A1, when tested along the <100> direction, exhibit remarkably high values of activation energy for creep. Along with evidence from dislocation structures, it is likely that there is a change in the dislocation core structure upon Cr addition.


1992 ◽  
Vol 7 (9) ◽  
pp. 2360-2364 ◽  
Author(s):  
J.L. Routbort ◽  
K.C. Goretta ◽  
D.J. Miller ◽  
D.B. Kazelas ◽  
C. Clauss ◽  
...  

Dense polycrystalline Bi2Sr1.7CaCu2Ox (2212) was deformed from 780–835 °C in oxygen partial pressures, Po2, of 103 to 2 × 104 Pa. Results could be divided into two stress regimes: one at lower stress in which the steady-state creep rate, ∊, was proportional to stress, γ, having an activation energy of 990 ± 190 kJ/mole and being independent of PO2, and another at higher stress in which ∊ was proportional to σn, with n ≍ 5–6. Transmission electron microscopy supported the interpretation that in the lower-stress viscous regime, creep was controlled by diffusion, whereas dislocation glide and microcracking were responsible for strain accommodation at higher stresses.


1958 ◽  
Vol 36 (11) ◽  
pp. 1445-1449 ◽  
Author(s):  
L. G. Bonar ◽  
G. B. Craig

The literature reports values ranging from 8000 to 26,000 cal per g-atom for the activation energy for the creep of tin. The present investigation analyzed the results of constant stress creep tests during steady state creep, and by means of temperature cycling. A value of approximately 9000 cal per g-atom for the creep of high purity tin in the temperature range 300 to 350° K was obtained.


1990 ◽  
Vol 213 ◽  
Author(s):  
Tohru Hayashi ◽  
Tetsumori Shinoda ◽  
Yoshinao Mishima ◽  
Tomoo Suzuki

ABSTRACTCompressive creep behavior is investigated In polycrystalline Ni3Al intermetallic compounds in which the focus is put on the effect of offstoichiometry and ternary additions of Ti, Ta, V and Co on the creep resistance of the compounds. In all cases, the steady-state creep rate has the power-law type dependence on the applied stress. The stress exponent thereby obtained leads us to regard the creep behavior of the compound to be of the Class I type. It is shown that the creep resistance Increases with increasing Ni concentration on both sides of the stoichiometric Ni3Al composition and a discontinuity exists in the variation at stoichiometry. The gap at the discontinuity becomes clearer by the addition of ternary element in most cases as compared to the binary Ni3Al. Although the exact reason for the phenomenon is not clearly understood at present, it is shown that it could be interpreted by the concentration dependence of activation energy in the power-law type creep equation.


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