Influence of water on plastic deformation of olivine aggregates: 2. Dislocation creep regime
Влияние воды на пластическую деформацию агрегатов оливина: 2. Режим дислокационной ползучести
2000-09-10
SCID: 54.1/ukedpy8a
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dislocation climbdislocation creepolivine aggregatessilicon interstitial diffusionwater fugacity
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Abstract (AI)
Triaxial compressive creep experiments have been conducted over a range of hydrous conditions to investigate the effect of water fugacity on the creep behavior of olivine aggregates in the dislocation creep regime. Samples synthesized from powders of San Carlos olivine were deformed at confining pressures of 100 to 450 MPa and temperatures between 1473 and 1573 K. Water was supplied by the dehydration of talc. Water fugacities of ∼80 to ∼520 MPa were obtained by varying the confining pressure under water‐saturated conditions with the oxygen fugacity buffered at Ni/NiO. Sancles were deformed at differential stresses of ∼20 to 230 MPa. The transition from diffusion creep to dislocation creep occurs near 100 MPa for both the hydrous case and the anhydrous case. Under hydrous conditions creep experiments yield a stress exponent of n ≈ 3 and an activation energy of Q ≈ 470 kJ/mol. The creep rate of olivine is enhanced significantly with the presence of water. At a water fugacity of ∼300 MPa, samples crept ∼5–6 times faster than those deformed under anhydrous conditions at similar differential stresses and temperatures. Within the range of water fugacity investigated, the strain rate is proportional to water fugacity to the 0.69 to 1.25 power, assuming values for the activation volume of 0 to 38×10 −6 m 3 /mol, respectively. We argue that water influences creep rate primarily through its effect on the concentrations of intrinsic point defects and hence on ionic diffusion and dislocation climb. With increasing water fugacity the charge neutrality condition changes from [Fe Me • ] = 2[V Me ″] to [Fe Me • ] = [H Me ′]. For the latter charge neutrality condition the concentration of silicon interstitials is proportional to , suggesting that under hydrous conditions dislocation climb is rate limited by diffusion of Si occurring by an interstitial mechanism. Our experimentally determined constitutive equation permits extrapolation from laboratory to mantle conditions in order to assess the rheological behavior of regions of the upper mantle with different water contents, such as beneath a mid‐ocean ridge and in the mantle wedge above a subducting slab.
Key Findings
1
The transition from diffusion creep to dislocation creep occurs near 100 MPa under both hydrous and anhydrous conditions.
2
Under hydrous conditions, olivine dislocation creep follows a stress exponent of approximately 3 and an activation energy of approximately 470 kJ/mol.
3
Water likely enhances creep by modifying intrinsic point-defect concentrations, promoting ionic diffusion and dislocation climb through an interstitial silicon-diffusion mechanism.
4
Water substantially accelerates olivine creep; at a water fugacity of approximately 300 MPa, creep is 5–6 times faster than under anhydrous conditions.
5
Within the investigated range, strain rate scales with water fugacity to the 0.69–1.25 power, depending on the assumed activation volume.
Research Object
olivine aggregates deforming in the dislocation creep regime under hydrous and anhydrous conditions
Research Subject
the influence of water fugacity on creep rate and deformation mechanisms, including point-defect concentrations, ionic diffusion, and dislocation climb
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2000-09-10
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