| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 673575 | Thermochimica Acta | 2013 | 8 Pages |
•TG/DSC analysis was conducted on magnesium-containing eutectic Li/Na eutectic carbonates.•Magnesium influence on the oxygen solubility properties of carbonate was also experimentally determined at 600 °C and 650 °C.•A reproducible partial decarbonation process in premelting region caused formation of magnesium oxycarbonate-like phases.•The acidobase buffering action of magnesium oxycarbonate species could explain the high basic/oxidizing properties of such carbonate melts.•A general correlation between thermal instability in premelting region and basic/oxidizing melt properties was established.
A comparative study on thermal behavior and oxygen solubility properties of eutectic 52/48 lithium/sodium carbonate salt containing minor additions of magnesium up to 10 mol% has been made in order to determine whether a general correlation between these two properties can be found or not. Consecutive TG/DSC heating/cooling thermal cycles carried out under alternating CO2 and N2 gas flows allowed to assign thermal events observed in the premelting region to a partial decarbonation process of the magnesium-alkali mixed carbonates. The observed decarbonation process at 460 °C is believed to come from initial stage of thermal decomposition of magnesium carbonate resulting in the metastable formation of magnesium oxycarbonate-like phases MgO·2MgCO3, in a similar manner as previously reported for lanthanum. Reversible formation and decomposition of the magnesium carbonate phase has been observed under a CO2 gas atmosphere. The intensity of the decomposition process shows a maximum for a 3 mol% MgO addition that gives also the highest oxygen solubility, suggesting therefore that instability thermal analysis in the premelting region can be considered as providing an effective measure of the basicity/oxidizing properties of alkali carbonate melts with magnesium or, in more general terms, with cations that are strong modifiers of the carbonate melt basicity through formation of soluble oxycarbonate phases.
