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American Mineralogist; February 2005; v. 90; no. 2-3; p. 441-447; DOI: 10.2138/am.2005.1740
© 2005 Mineralogical Society of America
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Molar absorptivities of OH and H2O in rhyolitic glass at room temperature and at 400–600 °C

Satoshi Okumura1,* and Satoru Nakashima1,2

1 Department of Earth and Planetary Sciences, Graduate School of Science and Engineering, Tokyo Institute of Technology, Meguro-ku, Tokyo 152-8551, Japan
2 Interactive Research Center of Science, Graduate School of Science and Engineering, Tokyo Institute of Technology, Meguro-ku, Tokyo 152-8551, Japan

Correspondence: * E-mail: sokumura{at}geo.titech.ac.jp

We determined near-infrared (NIR) molar absorptivities of hydroxyl group (4500 cm–1) and molecular water (5230 cm–1) in rhyolitic glasses at room temperature and at high temperature, 400–600 °C. Five rhyolitic glasses with 0.5–2.8 wt% total water were analyzed by FT-IR microspectroscopy at room temperature and at 50 °C intervals in the range of 400 to 600 °C using a heating stage. The total water contents in the rhyolitic glasses were measured by Karl-Fischer titration. Based on these data, the linear molar absorptivities of the 4500 and 5230 cm–1 bands at room temperature were determined to be 1.42 ± 0.12 and 1.75 ± 0.08 L/mol·cm, respectively. The integral molar absorptivities obtained are 285 ± 24 and 239 ± 11 L/mol·cm2 for the 4500 and 5230 cm–1 bands, respectively. These values can be used to determine the concentrations of hydroxyl group and molecular water in rhyolitic glass with 0.5–2.8 wt% total water at room temperature. The experimental results at high temperature show that the linear and integral molar absorptivities of the 4500 cm–1 band at 400–600 °C generally remain within 6% of the values at room temperature. On the other hand, the linear and integral molar absorptivities of the 5230 cm–1 band systematically decrease with increasing temperature in the ranges of 400 to 600 °C. These high-temperature molar absorptivities are useful for evaluating the water speciation in rhyolitic glass by in situ shigh-temperature IR microspectroscopy.




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