High pressure deformation experiments using solid confining media and Griggs piston-cylinder methods: Appraisal of stress and deformation in talc assemblies
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Attempts to calibrate mechanical results obtained in triaxial compression experiments using solid media assemblies in a Griggs piston-cylinder apparatus have failed to reveal a dependable relationship between results obtained using a talc assembly and results obtained with a gas triaxial deformation apparatus. Temperature-stepping experiments (600C-1000C) were performed on high-purity molybdenum (Mo) and a Ti-Zr-Mo alloy (TZM), pressurized by talc in a Griggs apparatus and by argon gas using a Heard apparatus. Apparent strengths of metal samples deformed at temperatures in the stability field of talc were at least 1500MPa (>6 times) greater than those determined in gas apparatus experiments, and they do not appear to follow any simple trend. At temperatures above talc dehydration, apparent strengths in talc assemblies were 500-800MPa (>2 1/2 times) greater. Total shortening strains of the metal samples measured after deformation in talc exceeded axial strains monitored during the triaxial deformation stage of the experiments by as much as 15-25%. A pressurization experiment performed on a TZM cylinder in talc, without engaging the load column, shows that samples can be shortened axially by the pressurization process. This test and a pressurization experiment conducted on a compound sample of Balsam Gap dunite and San Carlos olivine indicate that differential stresses within talc assemblies exceed the yield strengths of these materials during pressurization. Deformation of Balsam Gap dunite and San Carlos olivine during pressurization leads to complex microstructures, consisting of brittle faults, high dislocation densities, and small (10-40m) recrystallized grains. Experimental studies of deformation mechanisms and microstructures in samples deformed in strong solid confining media using Griggs piston-cylinder methods must therefore establish that the observed crystalline defects and microstructures are due to deformation at the controlled temperature, pressure, and strain rate conditions of the triaxial deformation, having replaced or substantially overprinted those developed during pressurization. 2012 Elsevier B.V.
