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High‐pressure behavior and stability of synthetic buetschliite K2Ca(CO3)2 up to 19 GPa and 300°C

The occurrence of buetschliite, K2Ca(CO3)2, as inclusions in mantle minerals, is considered as one of the keys to understanding phase relationships of dense carbonates and outlines the potential role of potassium carbonates in the Earth's deep carbon cycle. Within this scope, the high‐pressure...

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Bibliographic Details
Published in:Journal of Raman spectroscopy 2024-04, Vol.55 (4), p.517-524
Main Authors: Likhacheva, Anna Yu, Miloš, Sofija, Romanenko, Alexandr V., Goryainov, Sergey V., Semerikova, Anna I., Rashchenko, Sergey V., Miletich, Ronald, Shatsky, Anton
Format: Article
Language:English
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Summary:The occurrence of buetschliite, K2Ca(CO3)2, as inclusions in mantle minerals, is considered as one of the keys to understanding phase relationships of dense carbonates and outlines the potential role of potassium carbonates in the Earth's deep carbon cycle. Within this scope, the high‐pressure behavior of synthetic buetschliite is characterized by in situ Raman spectroscopy up to 19 GPa and 300°C. Up to 6 GPa, the compression is regular, then the splitting of some of the lattice and internal modes defines the transition to a low‐symmetry phase, in analogy to that observed previously in K2Mg(CO3)2. The temperature rise to 300°C shifts the transition pressure from ~6 to ~8 GPa, but on the whole, it does not change the high‐pressure behavior of K2Ca(CO3)2. The observed pressure‐induced spectral changes are fully reversible at room and elevated temperature. The findings show the expansion of buetschliite baric stability with temperature, which confirms its importance as a constituent of carbonate inclusions in deep minerals. Buetschliite occurring as inclusions in deep minerals is a key to understanding phase relationships of dense carbonates and their role in the Earth's deep carbon cycle. In situ Raman spectroscopy revealed positive slope of the transition to a lower‐symmetry phase. Such expansion of the buetschliite baric stability emphasizes its importance as a constituent of deep carbonates associations.
ISSN:0377-0486
1097-4555
DOI:10.1002/jrs.6654