Molecular H2O as carrier for oxygen diffusion in hydrous silicate melts

Research output: Contribution to journalArticleResearchpeer review

Authors

  • H. Behrens
  • Y. Zhang
  • M. Leschik
  • M. Wiedenbeck
  • G. Heide
  • G. H. Frischat

Research Organisations

External Research Organisations

  • University of Michigan
  • Clausthal University of Technology
  • Helmholtz Centre Potsdam - German Research Centre for Geosciences (GFZ)
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Details

Original languageEnglish
Pages (from-to)69-76
Number of pages8
JournalEarth and Planetary Science Letters
Volume254
Issue number1-2
Early online date22 Dec 2006
Publication statusPublished - 15 Feb 2007

Abstract

Dissolved water is known to dramatically enhance oxygen diffusion in silicate melts, glasses and minerals. A quantitative theory has been developed to explain this phenomenon by transport via molecular H2O diffusion [Y. Zhang, E.M. Stolper, G.J. Wasserburg, Diffusion of a multi-species component and its role in the diffusion of water and oxygen in silicates, Earth Planet. Sci. Lett., 103 (1991) 228-240.]. Here we report experimental confirmation of the theory for rhyolitic melts by measuring both H2O and 18O diffusion profiles in a single experiment. In sorption experiments at 100 MPa and temperatures from 1041 to 1136 K isotopically enriched water diffused into doubly polished rhyolitic glass wafers. H2O profiles were analyzed by infrared spectroscopy and 18O profiles by SIMS. 18O diffusivities were found to be 1-2 orders of magnitude slower than bulk water diffusivities but 3-4 orders of magnitude faster than Eyring diffusivities calculated from viscosity. The data show that oxygen "self" diffusion under hydrothermal conditions is due to molecular H2O diffusion, not due to the self diffusion of oxygen itself. With this confirmation, experimental data on H2O diffusion in silicate melts can be used to infer 18O diffusion under hydrothermal conditions, and hydrothermal oxygen diffusion data in silicate minerals can be used to infer H2O diffusivity, as long as the concentration or solubility of H2O in the given phase is known.

Keywords

    HO diffusion, hydrous silicate melts, oxygen and hydrogen isotopes, oxygen diffusion, rhyolite

ASJC Scopus subject areas

Cite this

Molecular H2O as carrier for oxygen diffusion in hydrous silicate melts. / Behrens, H.; Zhang, Y.; Leschik, M. et al.
In: Earth and Planetary Science Letters, Vol. 254, No. 1-2, 15.02.2007, p. 69-76.

Research output: Contribution to journalArticleResearchpeer review

Behrens, H, Zhang, Y, Leschik, M, Wiedenbeck, M, Heide, G & Frischat, GH 2007, 'Molecular H2O as carrier for oxygen diffusion in hydrous silicate melts', Earth and Planetary Science Letters, vol. 254, no. 1-2, pp. 69-76. https://doi.org/10.1016/j.epsl.2006.11.021
Behrens, H., Zhang, Y., Leschik, M., Wiedenbeck, M., Heide, G., & Frischat, G. H. (2007). Molecular H2O as carrier for oxygen diffusion in hydrous silicate melts. Earth and Planetary Science Letters, 254(1-2), 69-76. https://doi.org/10.1016/j.epsl.2006.11.021
Behrens H, Zhang Y, Leschik M, Wiedenbeck M, Heide G, Frischat GH. Molecular H2O as carrier for oxygen diffusion in hydrous silicate melts. Earth and Planetary Science Letters. 2007 Feb 15;254(1-2):69-76. Epub 2006 Dec 22. doi: 10.1016/j.epsl.2006.11.021
Behrens, H. ; Zhang, Y. ; Leschik, M. et al. / Molecular H2O as carrier for oxygen diffusion in hydrous silicate melts. In: Earth and Planetary Science Letters. 2007 ; Vol. 254, No. 1-2. pp. 69-76.
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AU - Behrens, H.

AU - Zhang, Y.

AU - Leschik, M.

AU - Wiedenbeck, M.

AU - Heide, G.

AU - Frischat, G. H.

N1 - Funding Information: This study was supported by German DFG and the US NSF (EAR-0228752; EAR-0537598). We thank the constructive and insightful comments of an anonymous reviewer.

PY - 2007/2/15

Y1 - 2007/2/15

N2 - Dissolved water is known to dramatically enhance oxygen diffusion in silicate melts, glasses and minerals. A quantitative theory has been developed to explain this phenomenon by transport via molecular H2O diffusion [Y. Zhang, E.M. Stolper, G.J. Wasserburg, Diffusion of a multi-species component and its role in the diffusion of water and oxygen in silicates, Earth Planet. Sci. Lett., 103 (1991) 228-240.]. Here we report experimental confirmation of the theory for rhyolitic melts by measuring both H2O and 18O diffusion profiles in a single experiment. In sorption experiments at 100 MPa and temperatures from 1041 to 1136 K isotopically enriched water diffused into doubly polished rhyolitic glass wafers. H2O profiles were analyzed by infrared spectroscopy and 18O profiles by SIMS. 18O diffusivities were found to be 1-2 orders of magnitude slower than bulk water diffusivities but 3-4 orders of magnitude faster than Eyring diffusivities calculated from viscosity. The data show that oxygen "self" diffusion under hydrothermal conditions is due to molecular H2O diffusion, not due to the self diffusion of oxygen itself. With this confirmation, experimental data on H2O diffusion in silicate melts can be used to infer 18O diffusion under hydrothermal conditions, and hydrothermal oxygen diffusion data in silicate minerals can be used to infer H2O diffusivity, as long as the concentration or solubility of H2O in the given phase is known.

AB - Dissolved water is known to dramatically enhance oxygen diffusion in silicate melts, glasses and minerals. A quantitative theory has been developed to explain this phenomenon by transport via molecular H2O diffusion [Y. Zhang, E.M. Stolper, G.J. Wasserburg, Diffusion of a multi-species component and its role in the diffusion of water and oxygen in silicates, Earth Planet. Sci. Lett., 103 (1991) 228-240.]. Here we report experimental confirmation of the theory for rhyolitic melts by measuring both H2O and 18O diffusion profiles in a single experiment. In sorption experiments at 100 MPa and temperatures from 1041 to 1136 K isotopically enriched water diffused into doubly polished rhyolitic glass wafers. H2O profiles were analyzed by infrared spectroscopy and 18O profiles by SIMS. 18O diffusivities were found to be 1-2 orders of magnitude slower than bulk water diffusivities but 3-4 orders of magnitude faster than Eyring diffusivities calculated from viscosity. The data show that oxygen "self" diffusion under hydrothermal conditions is due to molecular H2O diffusion, not due to the self diffusion of oxygen itself. With this confirmation, experimental data on H2O diffusion in silicate melts can be used to infer 18O diffusion under hydrothermal conditions, and hydrothermal oxygen diffusion data in silicate minerals can be used to infer H2O diffusivity, as long as the concentration or solubility of H2O in the given phase is known.

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