Abstract

AbstractDynamic recrystallization and phase mixing are considered to be important processes in ductile shear zone formation, as they collectively enable a permanent transition to the strain‐weakening, grain‐size sensitive deformation regime. While dynamic recrystallization is well understood, the underlying physical processes and timescales required for phase mixing remain enigmatic. Here, we present results from high‐strain phase mixing experiments on calcite‐anhydrite composites. A poorly mixed starting material was synthesized from fine‐grained calcite and anhydrite powders. Samples were deformed in the Large Volume Torsion apparatus at 500°C and shear strain rates of 5 × 10−5 to 5 × 10−4 s−1, to finite shear strains of up to γ = 57. Microstructural evolution is quantified through analysis of backscattered electron images and electron backscatter diffraction data. During deformation, polycrystalline domains of the individual phases are geometrically stretched and thinned, causing an increase in the spatial density of interphase boundaries. At moderate shear strains (γ ≥ 6), domains are so severely thinned that they become “monolayers” of only one or two grain's width and form a thin compositional layering. Monolayer formation is accompanied by a critical increase in the degree of grain boundary pinning and, consequently, grain‐size reduction below the theoretical limit established by the grain‐size piezometer or deformation mechanism field boundary. Ultimately, monolayers neck and disaggregate at high strains (17 <γ <57) to complete the phase mixing process. This “geometric” phase mixing mechanism is consistent with observations of mylonites, where layer (i.e., foliation) formation is associated with strain localization, and layers are ultimately destroyed at the mylonite‐ultramylonite transition.

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