Experimental deformation of fine-grained anhydrite: Evidence for dislocation and diffusion creep

1995 ◽  
Vol 100 (B8) ◽  
pp. 15425-15440 ◽  
Author(s):  
Lisa N. Dell'Angelo ◽  
David L. Olgaard
Geosciences ◽  
2019 ◽  
Vol 9 (10) ◽  
pp. 420
Author(s):  
Joseph W. Millard ◽  
Caleb W. Holyoke ◽  
Rachel K. Wells ◽  
Cole Blasko ◽  
Andreas K. Kronenberg ◽  
...  

We determined the activation volumes (V*) for polycrystalline magnesite with grain sizes of 2 and 80 µm deforming by low temperature plasticity (LTP) mechanisms (kinking and dislocation glide), diffusion creep, and dislocation creep at temperatures of 500, 750, and 900 °C, respectively, and a strain rate of 1–2 × 10−5 s−1 at effective pressures of 2.9–7.5 GPa in a D-DIA and 0.76 GPa in a Griggs apparatus. In each set of experiments performed at a given temperature, the strength of magnesite increases with increasing pressure. Microstructures of fine-grained magnesite deformed at 500 °C and 750 °C are consistent with deformation by LTP mechanisms and diffusion creep, respectively. Microstructures of coarse-grained magnesite deformed at 900 °C are consistent with deformation by dislocation creep. Pressure dependencies of magnesite flow laws for LTP, diffusion creep, and dislocation creep are given by activation volumes of 34 (± 7), 2 (± 1), and 10 (± 5) × 10−6 m3/mol, respectively. Addition of these activation volumes to previously determined flow laws predicts magnesite strength to be much lower than the flow strength of olivine at all subduction zone depths of the upper mantle. Thus, subducting oceanic lithosphere that has been partially carbonated by reaction with CO2-bearing fluids may deform at lowered stresses where magnesite is present, possibly resulting in strain localization and unstable run-away shear.


Ceramics ◽  
2021 ◽  
Vol 4 (2) ◽  
pp. 331-363
Author(s):  
Eugeniy Lantcev ◽  
Aleksey Nokhrin ◽  
Nataliya Malekhonova ◽  
Maksim Boldin ◽  
Vladimir Chuvil'deev ◽  
...  

This study investigates the impact of carbon on the kinetics of the spark plasma sintering (SPS) of nano- and submicron powders WC-10wt.%Co. Carbon, in the form of graphite, was introduced into powders by mixing. The activation energy of solid-phase sintering was determined for the conditions of isothermal and continuous heating. It has been demonstrated that increasing the carbon content leads to a decrease in the fraction of η-phase particles and a shift of the shrinkage curve towards lower heating temperatures. It has been established that increasing the graphite content in nano- and submicron powders has no significant effect on the SPS activation energy for “mid-range” heating temperatures, QS(I). The value of QS(I) is close to the activation energy of grain-boundary diffusion in cobalt. It has been demonstrated that increasing the content of graphite leads to a significant decrease in the SPS activation energy, QS(II), for “higher-range” heating temperatures due to lower concentration of tungsten atoms in cobalt-based γ-phase. It has been established that the sintering kinetics of fine-grained WC-Co hard alloys is limited by the intensity of diffusion creep of cobalt (Coble creep).


2000 ◽  
Vol 105 (B11) ◽  
pp. 26017-26036 ◽  
Author(s):  
E. Rybacki ◽  
G. Dresen

1994 ◽  
Vol 40 (136) ◽  
pp. 566-568
Author(s):  
G. A. Kuehn ◽  
E. M. Schulson

AbstractExperiments have shown that tensile ductility of about 5% or more can be imparted to columnar, saline ice by pre-compressing the material by about 3.5%. This effect is similar to that observed in granular, fresh-water ice and is attributed to the operation of both dislocation creep and diffusion creep within that part of the matrix which recrystallized during the pre-compressive deformation.


2018 ◽  
Author(s):  
Alberto Ceccato ◽  
Luca Menegon ◽  
Giorgio Pennacchioni ◽  
Luiz Fernando Grafulha Morales

Abstract. At mid-crustal conditions, deformation of feldspar is mainly accomplished by a combination of fracturing, dissolution/precipitation and reaction-weakening mechanisms. In particular, K-feldspar is reaction-weakened by formation of strain-induced myrmekite – a fine-grained symplectite of plagioclase and quartz. Here we investigate with EBSD the microstructure of a granodiorite mylonite, developed at 420–460 °C during cooling of the Rieserferner pluton (Eastern Alps), to assess the microstructural processes and the role of weakening associated with myrmekite development. Our analysis shows that the crystallographic orientation of the plagioclase of pristine myrmekite was controlled by that of the replaced K-feldspar. Myrmekite nucleation resulted in both grain size reduction and ordered phase mixing by heterogeneous nucleation of quartz and plagioclase. The fine grain size of sheared myrmekite promoted grain size-sensitive creep mechanisms including fluid-assisted grain boundary sliding in plagioclase, coupled with heterogeneous nucleation of quartz within creep cavitation pores. Flow laws calculated for monomineralic quartz, feldspar, and quartz + plagioclase aggregates (sheared myrmekite), show that during mylonitization at 450 °C, grain-size-sensitive creep in sheared myrmekite accommodated strain rates several orders of magnitude higher than monomineralic quartz layers deforming by dislocation creep. Therefore, diffusion creep and grain size-sensitive processes contributed significantly to bulk rock weakening during mylonitization. Our results have implications for modelling the rheology of the mid-upper continental (felsic) crust.


2020 ◽  
Vol 175 (12) ◽  
Author(s):  
John Wheeler

AbstractThe interplay between stress and chemical processes is a fundamental aspect of how rocks evolve, relevant for understanding fracturing due to metamorphic volume change, deformation by pressure solution and diffusion creep, and the effects of stress on mineral reactions in crust and mantle. There is no agreed microscale theory for how stress and chemistry interact, so here I review support from eight different types of the experiment for a relationship between stress and chemistry which is specific to individual interfaces: (chemical potential) = (Helmholtz free energy) + (normal stress at interface) × (molar volume). The experiments encompass temperatures from -100 to 1300 degrees C and pressures from 1 bar to 1.8 GPa. The equation applies to boundaries with fluid and to incoherent solid–solid boundaries. It is broadly in accord with experiments that describe the behaviours of free and stressed crystal faces next to solutions, that document flow laws for pressure solution and diffusion creep, that address polymorphic transformations under stress, and that investigate volume changes in solid-state reactions. The accord is not in all cases quantitative, but the equation is still used to assist the explanation. An implication is that the chemical potential varies depending on the interface, so there is no unique driving force for reaction in stressed systems. Instead, the overall evolution will be determined by combinations of reaction pathways and kinetic factors. The equation described here should be a foundation for grain-scale models, which are a prerequisite for predicting larger scale Earth behaviour when stress and chemical processes interact. It is relevant for all depths in the Earth from the uppermost crust (pressure solution in basin compaction, creep on faults), reactive fluid flow systems (serpentinisation), the deeper crust (orogenic metamorphism), the upper mantle (diffusion creep), the transition zone (phase changes in stressed subducting slabs) to the lower mantle and core mantle boundary (diffusion creep).


2020 ◽  
Author(s):  
Lucille Nègre ◽  
Holger Stünitz ◽  
Hugues Raimbourg ◽  
Jacques Précigout ◽  
Petr Jeřábek ◽  
...  

<p>The ability of water to enhance plastic deformation of a quartz aggregate has been experimentally demonstrated during the sixties (e.g. Griggs and Blacic 1965), however the processes involved are still questioned. Notably the processes combining the effect of water and pressure during the deformation are still not completely understood. Pressure strongly influences the strength of fine-grained (3.6 - 4.9 µm) wet quartz aggregates (Kronenberg and Tullis 1984), where diffusion creep operates (Fukuda et al. 2018) but its effect on coarser-grained material expected to deform only by dislocation creep is not well constrained. To re-assess the effect of pressure on quartz crystal plastic deformation, natural wet quartzite samples from the Tana quarry in northern Norway (grain size ≈ 150 µm) have been deformed using a Griggs-type apparatus at varying confining pressures (from 0.6 to 2.0 GPa). All the samples with 0.1 wt. % H<sub>2</sub>O added were shortened coaxially up to 30% strain at constant strain rate (≈10<sup>-6</sup> s<sup>-1</sup>) and temperature (900°C).</p><p>All mechanical records show that quartzite flow stresses decrease systematically with increasing pressure. These results allow to determine the strength of quartzite as a function of water fugacity, such as introduced in the flow law by Kohlstedt et al. (1995) to account for both pressure and water effects. In our case, the fugacity coefficient is m≈1 when using a stress exponent of n=2.</p><p>Microstructure and image analyses of samples reveal that the bulk strain results mainly from crystal plastic deformation of original grains whereas the recrystallization processes are limited volumetrically (less than 5%) and restricted to the boundaries of original grains. Deformation is not strongly partitioned into recrystallized domains compared to flattened original grains. Optical and SEM-cathodoluminescence images revealed the presence of cracks in conjunction with recrystallization (even for high-pressure samples) and associated chemical/fluid interaction, but the cracks do not contribute significantly to the bulk strain of the samples.</p><p>In order to determine the amount of water used for the deformation and the redistribution of H<sub>2</sub>O during deformation, the H<sub>2</sub>O content of the quartzite has been calculated from FTIR (Fourier Transform InfraRed spectroscopy) measurements for both, grain interiors and grain boundaries. The H<sub>2</sub>O concentrations decrease inside grains with the onset of deformation with respect to the starting material. H<sub>2</sub>O is primarily stored in the grain boundary region. There is no systematic correlation with pressure. Thus, pressure dependence of H<sub>2</sub>O weakening is not restricted to fine-grained materials at high pressure and temperature. Deformation redistributes water from the grain interiors to their grain boundaries.</p><p>References:<br>Fukuda, J., Holyoke III, C.W., and Kronenberg, A.K. (2018). J. Geophysical Res.: Solid Earth, 123(6), 4676-4696.<br>Griggs, D. T., and Blacic J. D. (1965). Science, 147(3655), 292‑295.<br>Kohlstedt, D. L., Evans B., and Mackwell S. J. (1995). J. Geophysical Res.: Solid Earth, 100(B9), 17587-17602.<br>Kronenberg, A. K., and Tullis J. (1984). J. Geophysical Res.: Solid Earth, 89(B6), 4281‑4297.</p>


Solid Earth ◽  
2018 ◽  
Vol 9 (6) ◽  
pp. 1399-1419 ◽  
Author(s):  
Alberto Ceccato ◽  
Luca Menegon ◽  
Giorgio Pennacchioni ◽  
Luiz Fernando Grafulha Morales

Abstract. At mid-crustal conditions, deformation of feldspar is mainly accommodated by a combination of fracturing, dissolution–precipitation, and reaction-weakening mechanisms. In particular, K-feldspar is reaction-weakened by the formation of strain-induced myrmekite – a fine-grained symplectite of plagioclase and quartz. Here we use electron backscattered diffraction to (i) investigate the microstructure of a granodiorite mylonite, developed at  ∼ 450 °C during cooling of the Rieserferner pluton (Eastern Alps); and (ii) assess the microstructural processes and the weakening associated with myrmekite development. Our analysis shows that the crystallographic orientation of plagioclase in pristine myrmekite was controlled by that of the replaced K-feldspar. Myrmekite nucleation resulted in both grain-size reduction and anti-clustered phase mixing by heterogeneous nucleation of quartz and plagioclase. The fine grain size of sheared myrmekite promoted grain-size-sensitive creep mechanisms including fluid-assisted grain boundary sliding in plagioclase, coupled with heterogeneous nucleation of quartz within creep cavitation pores. Flow laws, calculated for monomineralic quartz, feldspar, and quartz + plagioclase aggregates (sheared myrmekite) during deformation at 450 °C, show that grain-size-sensitive creep in sheared myrmekite accommodated strain rates several orders of magnitude higher than monomineralic quartz layers deforming by dislocation creep. Therefore, diffusion creep and grain-size-sensitive processes contributed significantly to bulk rock weakening during mylonitization. Our results have implications for modelling the rheology of the felsic middle crust.


Sign in / Sign up

Export Citation Format

Share Document