Viscosity of Iron-rich Silicate Melts by Falling Sphere Viscometry at High Pressure

Viscosity of Iron-rich Silicate Melts by Falling Sphere Viscometry at High Pressure

Author: Paul Michael Edwards

Publisher:

Published: 2019

Total Pages:

ISBN-13: 9781392212257

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Falling sphere viscometry at high pressures and temperatures is used to constrain the viscosity of iron-rich silicate liquids (natural and synthetic CaFeSi2O6), approximating pyroxenitic melts in the Earth’s mantle. In-situ falling sphere viscometry experiments are conducted using synchrotron radiation and the multi-anvil apparatus to record in real-time the motion of a small Re sphere falling through the melt at high pressure and temperature. Terminal velocity is determined from sphere position versus time plots and used, together with constraints on sphere diameter, sphere and melt density and capsule geometry, to compute melt viscosity from the Stokes equation. Experiments were conducted at the GSECARS 13-ID-D beamline at the Advanced Photon Source, Argonne National Lab in the T-25 multi-anvil apparatus. For this work a new in-situ falling sphere assembly was developed with a double reservoir capsule permitting the drop of the Re sphere from the upper reservoir of refractory materials into superliquidus melt in the low reservoir. This configuration enables viscosity to be determined over a range of superliquidus temperatures at a given pressure. Hedenbergite melt viscosity is found to vary between 0.45 Pa∙s to 0.05 Pa∙s from 1 to 7 GPa and 1760 to 2130 K. There are no significant differences in superliquidus viscosities for the natural and synthetic compositions. These new data are combined with published data on enstatite, wollastonite, and diopside liquids to estimate the viscosity of pyroxenitic melts up to 7 GPa. These results show that pyroxenite liquids have lower viscosity and weaker pressure dependence than basaltic melts at upper mantle conditions. Considering the densities of pyroxenitic and basaltic melts in the upper mantle, we find that pyroxenite melts have higher mobility than basaltic melts and thus are expected to segregate more readily that basaltic melt from a heterogeneous mantle source during partial melting by adiabatic decompression of upwelling mantle.


Silicate Glasses and Melts

Silicate Glasses and Melts

Author: Bjorn Mysen

Publisher: Elsevier

Published: 2005-06-16

Total Pages: 561

ISBN-13: 0080457711

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This book describes the structure-property-composition relationships for silicate glasses and melts of industrial and geological interest. From Antiquity to the 20th century, an introductory chapter presents this subject in a historical perspective. Basic concepts are then discussed in three chapters where attention is paid to the glass transition and its various consequences on melt and glass properties, to the structural and physical differences between amorphous and crystalline silicates, and to the mutual relationships between local order, energetics and physical properties. With pure SiO2 as a starting point, compositions of increasing chemical complexity are successively dealt with in a dozen chapters. The effects of network-modifying cations on structure and properties are first exemplified by alkali and alkaline earth elements. The specific influence of aluminum, iron, titanium, and phosphorus are then reviewed. With water, volatiles in the system COHS, noble gases, and halogens, the effects of volatile components are also described. The last chapter explains how the results obtained on simpler melts can be applied to chemically complex systems. In each chapter, physical and chemical properties are described first and followed by a review of glass and melt structure. When possible, pressure effects are also considered. *From SiO2 to complex silicate compositions, the physical and chemical properties of melts and glasses of geological and industrial interest*Structural characterization of melts and glasses, from ambient to high pressure and temperature*From basic concepts to an advanced level, a consistent description of the structure-property-composition relationships in glasses and melts