Journal
GEOCHIMICA ET COSMOCHIMICA ACTA
Volume 97, Issue -, Pages 1-23Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.gca.2012.08.035
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Funding
- European Community [PIEF-GA-2008-220926]
- European Research Council [279790]
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We present here new experimental data on H2O-CO2 solubility in mafic melts with variable chemical compositions (alkali basalt, lamproite and kamafugite) that extend the existing database. We show that potassium and calcium-rich melts can dissolve similar to 1 wt% CO2 at 3500 bar (350 MPa) and 1200 degrees C, whereas conventional models predict solubilities of 0.2-0.5 wt%, under similar P-T conditions. These new data, together with those in the literature, stress the fundamental control of melt chemical composition on CO2 solubility. We present a semi-empirical H2O-CO2 solubility model for mafic melts, which employs simplified concepts of gas-melt thermodynamics coupled with a parameterization of both chemical composition and structure of the silicate melt. The model is calibrated on a selected database consisting of 289 experiments with 44 different mafic compositions. Statistical analyses of the experimental data indicate that, in mafic melts, the chemical composition and therefore the structure of the melt plays a fundamental role in CO2 solubility. CO2 solubility strongly depends on the amount of non-bridging oxygen per oxygen (NBO/O) in the melt, but the nature of the cation bonded to NBO is also critical. Alkalis (Na + K) bonded to NBO result in a strong enhancement of CO2 solubility, whereas Ca has a more moderate effect. Mg and Fe bonded to NBO have the weakest effect on CO2 solubility. Finally, we modelled the effect of water and concluded that H2O dissolution in the melt enhances CO2 solubility most likely by triggering NBO formation. In contrast with CO2 but in agreement with earlier findings, H2O solubility in mafic melts is negligibly affected by melt composition and structure: it only shows a weak correlation with NBO/O. (C) 2012 Elsevier Ltd. All rights reserved.
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