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Updated: Jul 7, 2026

Synthesis and Microdiffraction at Extreme Pressures and Temperatures
Published on: October 7, 2013
An experimental system for time-resolved x-ray diffraction of deforming silicate melt at high temperature
Satoshi Okumura1, Kentaro Uesugi2, Tatsuya Sakamaki1
1Division of Earth and Planetary Materials Science, Department of Earth Science, Graduate School of Science, Tohoku University, Sendai, Miyagi 980-8578, Japan.
Abstract:
Rheological behavior of silicate melts controls the dynamics of volcanic eruptions. Previous experimental studies have investigated melt viscosity and found non-Newtonian behavior of the melt under a high shear rate. However, the relationship between macroscopic rheology and atomic-scale behavior under shear remains unclear. We developed an experimental system for time-resolved x-ray diffraction (XRD) at high temperature to investigate the atomic-scale structural change in melts under shear. The manufactured deformation apparatus and heating furnace were set on the synchrotron radiation x-ray beamline (BL20XU) of SPring-8; the XRD pattern of the melt at high temperature could be observed using this system because the furnace mainly consists of a boron nitride cylinder with high x-ray transmittance. Here, we report results of fiber elongation experiments for a soda-lime melt. Melt fibers with ∼0.7 mm in diameter and ∼27 mm long were elongated at 100 µm sec-1 at temperatures of 595 °C and 620 °C, and the XRD pattern was obtained every 100 msec. Brittle failure of the melt occurred at 595 °C, whereas the melt viscously elongated at 620 °C. The XRD patterns obtained during elongation did not indicate any clear change immediately before brittle failure. The intensity of the XRD pattern decreased with the elongation at 620 °C, although there was no clear variation in its shape. These results indicate that the atomic-scale structure observed by XRD may not change during the elastic and viscous elongation of the soda-lime melt. This experimental system will be further developed and applied to more polymerized and natural silicate melts.
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