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• W1995205337 endingPage "107" @default.
• W1995205337 startingPage "93" @default.
• W1995205337 abstract "Activity coefficients of oxide components in the system CaO-MgO-Al2O3-SiO2 (CMAS) were calculated with the model of Berman (Berman R. G., “A thermodynamic model for multicomponent melts with application to the system CaO-MgO-Al2O3-SiO2,” Ph.D. dissertation, University of British Columbia, 1983) and used to explore large-scale relationships among these variables and between them and the liquid composition. On the basis of Berman’s model, the natural logarithm of the activity coefficient of MgO, ln(γMgOLiq), and ln(γMgOLiq/γSiO2Liq) are nearly linear functions of ln(γCaOLiq). All three of these variables are simple functions of the optical basicity Λ with which they display minima near Λ ∼ 0.54 that are generated by liquids with low ratios of nonbridging to tetrahedral oxygens (NBO/T) (<0.3) and a mole fraction ratio, XSiO2Liq/XAl2O3Liq, in the range 4 to 20. Variations in ln(γCaOLiq) at constant Λ near the minimum are due mostly to liquids with (XCaOLiq + XMgOLiq)/XAl2O3Liq < 1. The correlations with optical basicity imply that the electron donor power is an important factor in determining the thermodynamic properties of aluminosilicate liquids. For a constant NBO/T, ln(γCaOLiq/γAl2O3Liq) and ln(γMgOLiqγAl2O3Liq) form curves in terms of XSiO2Liq/XAl2O3Liq. The same liquids that generate minima in the Λ plots are also associated with minima in ln(γCaOLiqγAl2O3Liq) and ln(γMgOLiqγAl2O3Liq) as a function of XSiO2Liq/XAl2O3Liq. In addition, there are maxima or sharp changes in slope for NBO/T > 0.3, which occur for XSiO2Liq/XAl2O3Liq ranging from ∼0 to ∼6 and increase with increasing NBO/T. The systematic variations in activity coefficients as a function of composition and optical basicity reflect underlying shifts in speciation as the composition of the liquid is changed. On the basis of correlations among the activity coefficients, it is likely that the use of CaO, an exchange component such as SiMg−1 and two of MgO, CaAl2O4, or MgAl2O4 would yield significant savings in the number of parameters required to model the excess free energy surface of liquids over large portions of CMAS relative to the use of oxide end members. Systematic behavior of thermodynamic properties extends to small amounts of other elements dissolved in otherwise CMAS liquids. For example, ln(XFe2+Liq/XFe3+Liq) at constant oxygen fugacity is linearly correlated with ln(γCaOLiq). Similarly, ln(CS), where CS is the sulfide capacity is linearly correlated at constant temperature with each of the optical basicity, ln(aCaOLiq) and ln(γCaOLiq), although the correlation for the latter breaks down for low values of Λ. The well-known systematic behavior of sulfide capacity as a function of optical basicity for systems inside as well as outside CMAS suggests that ln(γCaSLiq) is also a simple function of optical basicity and that the relationships observed among the activity coefficients in CMAS may hold for more complex systems." @default.
• W1995205337 created "2016-06-24" @default.
• W1995205337 creator A5037138772 @default.
• W1995205337 date "2002-01-01" @default.
• W1995205337 modified "2023-09-23" @default.
• W1995205337 title "Role of basicity and tetrahedral speciation in controlling the thermodynamic properties of silicate liquids, part 1: the system CaO-MgO-Al 2 O 3 -SiO 2" @default.
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• W1995205337 doi "https://doi.org/10.1016/s0016-7037(01)00751-7" @default.
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