Mass transfer in the Earth’s interior: fluid-melt interaction in aluminosilicate–C–O–H–N systems at high pressure and temperature under oxidizing conditions

Understanding what governs the speciation in the C–O–H–N system aids our knowledge of how volatiles affect mass transfer processes in the Earth’s interior. Experiments with aluminosilicate melt + C–O–H–N volatiles were, therefore, carried out with Raman and infrared spectroscopy to 800 °C and near 700 MPa in situ in hydrothermal diamond anvil cells. The measurements were conducted in situ with the samples at the desired temperatures and pressures in order to avoid possible structural and compositional changes resulting from quenching to ambient conditions prior to analysis. Experiments were conducted without any reducing agent and with volatiles added as H2O, CO2, and N2 because both carbon and nitrogen can occur in different oxidation states. Volatiles dissolved in melt comprise H2O, CO3 , HCO3 , and molecular N2, whereas in the coexisting fluid, the species are H2O, CO2, CO3 , and N2. The HCO3 /CO3 2equilibrium in melts shift toward CO3 2groups with increasing temperature with ΔH = 114 ± 22 kJ/mol. In fluids, the CO2 abundance is essentially invariant with temperature and pressure. For fluid/melt partitioning, those of H2O and N2 are greater than 1 with temperature-dependence that yields ΔH values of − 6.5 ± 1.5 and − 19.6 ± 3.7 kJ/mol, respectively. Carbonate groups, CO3 2are favored by melt over fluid. Where redox conditions in the Earth’s interior exceed that near the QFM oxygen buffer (between NNO and MW buffers), N2 is the stable nitrogen species and as such acts as a diluent of both fluids and melts. For fluids, this lower silicate solubility, in turn, enhances alkalinity. This means that in such environments, the transport of components such as high field strength cations, will be enhanced. Effects of dissolved N2 on melt structure are considerably less than on fluid structure.