Water and the density of silicate glasses

Publikation: Beitrag in FachzeitschriftÜbersichtsarbeitForschungPeer-Review

Autoren

  • Pascal Richet
  • Alan Whittington
  • François Holtz
  • Harald Behrens
  • Susanne Ohlhorst
  • Max Wilke

Organisationseinheiten

Externe Organisationen

  • European Space Agency (ESA)
  • University of Illinois Urbana-Champaign (UIUC)
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Details

OriginalspracheEnglisch
Seiten (von - bis)337-347
Seitenumfang11
FachzeitschriftContributions to Mineralogy and Petrology
Jahrgang138
Ausgabenummer4
PublikationsstatusVeröffentlicht - 1 Apr. 2000

Abstract

A review of published and newly measured densities for 40 hydrous silicate glasses indicates that the room-temperature partial molar volume of water is 12.0 ± 0.5 cm3/mol. This value holds for simple or mineral compositions as well as for complex natural glasses, from rhyolite to tephrite compositions, prepared up to 10-20 kbar pressures and containing up to 7 wt% H2O. This volume does not vary either with the molar volume of the water-free silicate phase, with its degree of polymerization or with water speciation. Over a wide range of compositions, this constant value implies that the volume change for the reaction between hydroxyl ions and molecular water is zero and that, at least in glasses, speciation does not depend on pressure. Consistent with data from Ochs and Lange (1997, 1999), systematics in volume expansion for SiO2-M2O systems (M = H, Li, Na, K) suggests that the partial molar thermal expansion coefficient of H2O is about 4 x 10-5 K-1 in silicate glasses.

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Water and the density of silicate glasses. / Richet, Pascal; Whittington, Alan; Holtz, François et al.
in: Contributions to Mineralogy and Petrology, Jahrgang 138, Nr. 4, 01.04.2000, S. 337-347.

Publikation: Beitrag in FachzeitschriftÜbersichtsarbeitForschungPeer-Review

Richet, P, Whittington, A, Holtz, F, Behrens, H, Ohlhorst, S & Wilke, M 2000, 'Water and the density of silicate glasses', Contributions to Mineralogy and Petrology, Jg. 138, Nr. 4, S. 337-347. https://doi.org/10.1007/s004100050567
Richet, P., Whittington, A., Holtz, F., Behrens, H., Ohlhorst, S., & Wilke, M. (2000). Water and the density of silicate glasses. Contributions to Mineralogy and Petrology, 138(4), 337-347. https://doi.org/10.1007/s004100050567
Richet P, Whittington A, Holtz F, Behrens H, Ohlhorst S, Wilke M. Water and the density of silicate glasses. Contributions to Mineralogy and Petrology. 2000 Apr 1;138(4):337-347. doi: 10.1007/s004100050567
Richet, Pascal ; Whittington, Alan ; Holtz, François et al. / Water and the density of silicate glasses. in: Contributions to Mineralogy and Petrology. 2000 ; Jahrgang 138, Nr. 4. S. 337-347.
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AU - Whittington, Alan

AU - Holtz, François

AU - Behrens, Harald

AU - Ohlhorst, Susanne

AU - Wilke, Max

N1 - Copyright: Copyright 2017 Elsevier B.V., All rights reserved.

PY - 2000/4/1

Y1 - 2000/4/1

N2 - A review of published and newly measured densities for 40 hydrous silicate glasses indicates that the room-temperature partial molar volume of water is 12.0 ± 0.5 cm3/mol. This value holds for simple or mineral compositions as well as for complex natural glasses, from rhyolite to tephrite compositions, prepared up to 10-20 kbar pressures and containing up to 7 wt% H2O. This volume does not vary either with the molar volume of the water-free silicate phase, with its degree of polymerization or with water speciation. Over a wide range of compositions, this constant value implies that the volume change for the reaction between hydroxyl ions and molecular water is zero and that, at least in glasses, speciation does not depend on pressure. Consistent with data from Ochs and Lange (1997, 1999), systematics in volume expansion for SiO2-M2O systems (M = H, Li, Na, K) suggests that the partial molar thermal expansion coefficient of H2O is about 4 x 10-5 K-1 in silicate glasses.

AB - A review of published and newly measured densities for 40 hydrous silicate glasses indicates that the room-temperature partial molar volume of water is 12.0 ± 0.5 cm3/mol. This value holds for simple or mineral compositions as well as for complex natural glasses, from rhyolite to tephrite compositions, prepared up to 10-20 kbar pressures and containing up to 7 wt% H2O. This volume does not vary either with the molar volume of the water-free silicate phase, with its degree of polymerization or with water speciation. Over a wide range of compositions, this constant value implies that the volume change for the reaction between hydroxyl ions and molecular water is zero and that, at least in glasses, speciation does not depend on pressure. Consistent with data from Ochs and Lange (1997, 1999), systematics in volume expansion for SiO2-M2O systems (M = H, Li, Na, K) suggests that the partial molar thermal expansion coefficient of H2O is about 4 x 10-5 K-1 in silicate glasses.

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