ACTIVITIES OF NIO, FEO, AND O2- IN SILICATE MELTS

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dc.contributor.author Colson R.O.
dc.contributor.author Floden A.M.
dc.contributor.author Haugen T.R.
dc.contributor.author Malum K.M.
dc.contributor.author Sawarynski M.
dc.contributor.author Nermoe M.K.B.
dc.contributor.author Jacobs K.E.
dc.contributor.author Holder D.
dc.date.accessioned 2023-11-18T10:28:19Z
dc.date.available 2023-11-18T10:28:19Z
dc.date.issued 2005
dc.identifier https://www.elibrary.ru/item.asp?id=12092194
dc.identifier.citation Geochimica et Cosmochimica Acta, 2005, 69, 12, 3061-3073
dc.identifier.issn 0016-7037
dc.identifier.uri https://repository.geologyscience.ru/handle/123456789/41880
dc.description.abstract We have measured activity coefficients for NiO and FeO in a variety of silicate melts (SiO2-CaO-MgO-Al2O3) using electrochemical methods similar to square wave voltametry. We report the activity of the oxide ion (aO2−) in one composition. Based on these measurements, we have constructed a model that predicts the variations in activity we observe, and also variations in NiO activity reported in the literature. Activity of metal-oxide components such as NiO and FeO in silicate melts can be understood by considering contributions from both the activity of the oxide ion and the activity of the cation through expressions of the type:aNiO=(aO2-)(aNi2+) andaFeO=(aO2-)(aFe2+) Based on measurements of aO2−, we find that aO2− is effectively modeled by the expression aO2− = 0.75·NBO2/BO (relative to a standard state of melt with the composition of diopside). Once the effects of variations in aO2− on the metal-oxide activity coefficient are accounted for, cation activities (aNi2+, aFe2+) can be modeled by an ideal-solution-like model in which the activity of Ni2+ or Fe2+ is related to its concentration among a subset of other cations with which it mixes (primarily other divalent cations). This model is successful in predicting NiO activities over the range of compositions 0.3
dc.title ACTIVITIES OF NIO, FEO, AND O2- IN SILICATE MELTS
dc.type Статья
dc.identifier.doi 10.1016/j.gca.2005.02.005


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