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Rapid CO(2) mineralisation into calcite at the CarbFix storage site quantified using calcium isotopes

The engineered removal of atmospheric CO(2) is now considered a key component of mitigating climate warming below 1.5 °C. Mineral carbonation is a potential negative emissions technique that, in the case of Iceland’s CarbFix experiment, precipitates dissolved CO(2) as carbonate minerals in basaltic...

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Detalles Bibliográficos
Autores principales: Pogge von Strandmann, Philip A. E., Burton, Kevin W., Snæbjörnsdóttir, Sandra O., Sigfússon, Bergur, Aradóttir, Edda S., Gunnarsson, Ingvi, Alfredsson, Helgi A., Mesfin, Kiflom G., Oelkers, Eric H., Gislason, Sigurður R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6491611/
https://www.ncbi.nlm.nih.gov/pubmed/31040283
http://dx.doi.org/10.1038/s41467-019-10003-8
Descripción
Sumario:The engineered removal of atmospheric CO(2) is now considered a key component of mitigating climate warming below 1.5 °C. Mineral carbonation is a potential negative emissions technique that, in the case of Iceland’s CarbFix experiment, precipitates dissolved CO(2) as carbonate minerals in basaltic groundwater settings. Here we use calcium (Ca) isotopes in both pre- and post-CO(2) injection waters to quantify the amount of carbonate precipitated, and hence CO(2) stored. Ca isotope ratios rapidly increase with the pH and calcite saturation state, indicating calcite precipitation. Calculations suggest that up to 93% of dissolved Ca is removed into calcite during certain phases of injection. In total, our results suggest that 165 ± 8.3 t CO(2) were precipitated into calcite, an overall carbon storage efficiency of 72 ± 5%. The success of this approach opens the potential for quantification of similar mineral carbonation efforts where drawdown rates cannot be estimated by other means.