THERMODYNAMIC MIXING PROPERTIES OF SODIUM SILICATE LIQUIDS AND IMPLICATIONS FOR LIQUID-LIQUID IMMISCIBILITY

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dc.contributor.author Hovis G.L.
dc.contributor.author Toplis M.J.
dc.contributor.author Richet P.
dc.date.accessioned 2022-07-09T04:44:25Z
dc.date.available 2022-07-09T04:44:25Z
dc.date.issued 2004
dc.identifier https://www.elibrary.ru/item.asp?id=31269323
dc.identifier.citation Chemical Geology, 2004, 213, 1-3, 173-186
dc.identifier.issn 0009-2541
dc.identifier.uri https://repository.geologyscience.ru/handle/123456789/38042
dc.description.abstract Enthalpies of solution have been measured for synthetic glasses in the SiO2–Na2O system from 0 to 50 mol% Na2O. The positive enthalpies of mixing determined for the compositional range between 0 and 33.3 mol% Na2O, combined with entropies for the same compositions based on ideal mixing involving Q4 and Q3 species, allowed us to calculate a liquid–liquid solvus in good agreement with the experimental data of Haller et al. [Haller, W., Blackburn, D.H., Simmons, J.H., 1974. Miscibility gaps in alkali–silicate binaries—data and thermodynamic interpretation. J. Am. Ceram. Soc. 57, 120–126]. This demonstrates a high degree of compatibility among the data for entropy, enthalpy, and phase equilibrium and also confirms the requirement of positive enthalpies of mixing for liquid immiscibility in the SiO2–Na2O system.
dc.title THERMODYNAMIC MIXING PROPERTIES OF SODIUM SILICATE LIQUIDS AND IMPLICATIONS FOR LIQUID-LIQUID IMMISCIBILITY
dc.type Статья


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