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The glass transition and the non-Arrhenian viscosity of carbonate melts

  • Donald B. Dingwell
  • , Kai Uwe Hess*
  • , Martin C. Wilding
  • , Richard A. Brooker
  • , Danilo Di Genova
  • , James W.E. Drewitt
  • , Mark Wilson
  • , Daniel Weidendorfer
  • *此作品的通讯作者
  • Ludwig Maximilian University of Munich
  • Materials and Engineering Research Institute
  • Sheffield Hallam University
  • U.K. Catalysis Hub
  • Rutherford Appleton Laboratory
  • Wills Memorial Building
  • School of Earth Sciences
  • Department of Theoretical Chemistry
  • University of Oxford

科研成果: 期刊稿件 › 文章 › 同行评审

摘要

We report the first calorimetric observation of the glass transition for a carbonate melt. A carbonate glass [55K2CO3-45MgCO3 (molar)] was quenched from 780 °C at 0.1 GPa. The activation energy of structural relaxation close to the glass transition was derived through a series of thermal treatments comprising excursions across the glass transition at different heating rates. Viscosities just above the glass transition temperature were obtained by applying a shift factor to the calorimetric results. These viscosity measurements (in the range of 109 Pa·s) at supercooled temperatures (ca. 230 °C) dramatically extend the temperature range of data for carbonates, which were previously restricted to superliquidus viscosities well below 1 Pa·s. Combining our calorimetrically derived results with published alkaline-earth carbonate melt viscosities at high temperatures yields a highly non-Arrhenian viscosity-temperature relationship and confirms that carbonate liquids are "fragile."Based on simulations, fragile behavior is also exhibited by Na2CO3 melt. In both cases, the fragility presumably relates to the formation of temperature-dependent low-dimensional structures and Vogel-Fulcher-Tammann (VFT) curves adequately describe the viscosity-temperature relationships of carbonate melts below 1000 °C.

源语言英语
页(从-至)1053-1064
页数12
期刊American Mineralogist
卷107
期6
DOI
出版状态已出版 - 1 6月 2022
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