Magnesium and carbon isotope fractionation during hydrated Mg-carbonate mineral phase transformations
•Mg and C isotope fractionation between hydrous Mg-carbonate minerals measured.•If dypingite forms from aqueous Mg2+, it would be preferentially enriched in 26Mg.•Isotopic composition of Mg-carbonate overwitten during mineral phase transformations.•Applications for using Mg and C isotopes as tracers...
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Veröffentlicht in: | Geochimica et cosmochimica acta 2021-01, Vol.293, p.507-524 |
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Zusammenfassung: | •Mg and C isotope fractionation between hydrous Mg-carbonate minerals measured.•If dypingite forms from aqueous Mg2+, it would be preferentially enriched in 26Mg.•Isotopic composition of Mg-carbonate overwitten during mineral phase transformations.•Applications for using Mg and C isotopes as tracers of carbon capture and storage.
The fractionation of carbon and magnesium isotopes is a potentially useful tracer of natural weathering in ultramafic catchments and engineered CO2 storage. To evaluate the use of carbon and magnesium isotopes as tracers of ultramafic weathering and CO2 storage, we assessed the carbon and magnesium isotope fractionation between hydrous Mg-carbonate minerals and fluid during a mineral phase transformation from nesquehonite [MgCO3·3H2O] to dypingite [Mg5(CO3)4(OH)2· ∼ 5–8H2O], two common products of ultramafic rock weathering. Batch reactor experiments containing nesquehonite were conducted at 5 °C, 25 °C, and 35 °C and the evolution of mineralogical composition, fluid composition, and isotopic composition were tracked over time. At 5 °C, the solid remained nesquehonite throughout the experiments, and isotopic equilibrium did not appear to be achieved between the solid and the fluid phase for either carbon or magnesium. At 25 °C, and 35 °C a transformation from nesquehonite to dypingite occurred by dissolution and re-precipitation, which resulted in extensive exchange of Mg and C between solid and fluid. The phase transformation caused the initial C and Mg isotopic composition of the solid phase to be overwritten. The extensive isotopic exchange during the phase transformation suggests C and Mg isotopes likely obtained approximate isotopic equilibrium between dypingite and fluid. For dypingite, the Δ13Cdyp-DIC was 4.74 ± 0.12‰ (VPDB) and 4.47 ± 0.17‰ (VPDB) at 25 and 35 °C, respectively. The Δmeas26Mgdyp-fluid between solid and the bulk fluid was −0.76‰, and −0.98 ± 0.08‰ for the 25 and 35 °C experiments, respectively. There was no clear impact of temperature on Mg or C isotope fractionation. The calculated Δcalc26Mgdyp-Mg2+ between dypingite and the Mg2+ aquo species rather than bulk aqueous Mg values were positive. This indicates that if dypingite is formed by the incorporation of the free Mg2+ ion in the solid, the solid is preferentially enriched in the isotope of higher mass (26Mg). This is opposite to anhydrous Mg-bearing carbonate minerals, which tend to be depleted in 26Mg relative to the forming fluid. These data will help |
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ISSN: | 0016-7037 1872-9533 |
DOI: | 10.1016/j.gca.2020.10.028 |