CARBON ISOTOPE FRACTIONATION IN SYNTHETIC MAGNESIAN CALCITE

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dc.contributor.author Jimenez-Lopez C.
dc.contributor.author Romanek C.S.
dc.contributor.author Caballero E.
dc.date.accessioned 2024-05-05T03:46:22Z
dc.date.available 2024-05-05T03:46:22Z
dc.date.issued 2006
dc.identifier https://elibrary.ru/item.asp?id=12091902
dc.identifier.citation Geochimica et Cosmochimica Acta, 2006, 70, 5, 1163-1171
dc.identifier.issn 0016-7037
dc.identifier.uri https://repository.geologyscience.ru/handle/123456789/43855
dc.description.abstract Mg-calcite was precipitated at 25 °C in closed system, free-drift experiments, from solutions containing NaHCO3, CaCl2 and MgCl2. The carbon stable isotope composition of bulk solid and solution were analyzed from subsamples collected during time course experiments of 24 h duration. Considering only the Mg-content and ?13C values for the bulk solid, the carbon isotope fractionation factor for the Mg-calcite-HCO3(aq)- system (as 103 ln ?Mg-cl-HCO3(aq)-) increased with average mol percentage of Mg (XMg) in the solid at a rate of (0.024 ? 0.011) per mol% MgCO3. Extrapolation of this relationship to the pure calcite end member yields a value of 0.82 ? 0.09, which is similar to published values for the calcite-HCO3(aq)- system. Although 103 ln ?Mg-cl-HCO3(aq)- did not vary for precipitation rates that ranged from 103.21 to 104.60 ?mol m-2 h-1, it was not possible to hold Mg-content of the solid constant, so kinetic effect on 103 ln ? could not be evaluated from these experiments. ? 2005 Elsevier Inc. All rights reserved.
dc.subject CALCITE
dc.subject CARBON ISOTOPE
dc.subject ISOTOPIC FRACTIONATION
dc.subject MAGNESIUM
dc.subject MARINE ENVIRONMENT
dc.title CARBON ISOTOPE FRACTIONATION IN SYNTHETIC MAGNESIAN CALCITE
dc.type Статья
dc.identifier.doi 10.1016/j.gca.2005.11.005


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