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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