Monazite saturation in carbonatite melts at crustal and upper mantle conditions

Monazite (XPO4 where X = light rare earth element) is one of the most important ore minerals for rare earth elements (REE) mined from carbonatites. This study explores the influence of pressure, temperature and melt composition on the solubility of monazite in carbonate melt using piston cylinder experiments. We aim to understand how such a highly soluble phosphate mineral may sometimes crystallise from carbonatite magma and form economic deposits of REE. Our findings reveal that the solubility of monazite in a sodic-dolomitic carbonate melt is high over the entire pressure (1.0–2.0 GPa), temperature (1000-1450˚C), and compositional space (Na2O-CaO-MgO-SiO2-F) of our study. It increases from ∼ 26 to ∼ 61 wt% CePO4 equivalent over the temperature range of 1000–1450 °C at 2 GPa. However, the solubility product constant (lnKsp) decreases by approximately ∼ 23 % and 21 % equivalent with increasing melt SiO2 (from 0 to ∼ 18 wt% melt SiO2) at 1275 °C and fluoride (from 0 to ∼ 5 wt% melt F-) concentrations at 1100 °C respectively. Variations in melt Ca# (atomic Ca/(Mg + Ca) = 0.2–1.0) and pressure (1.0–2.0 GPa) have negligible impacts on monazite solubility. We use the experimental data to formulate an empirical model relating the solubility product constant (Ksp) of monazite in carbonate melt to temperature and melt compositional parameters: lnKsp=lnREE2O3melt.P2O5melt=1.310.50-[Formula presented]-3.35(0.34)×SiO2-1.68(0.34)×F where [] represents the mole fractions of oxides in the melt of the rare earth elements, phosphorus and silicon, and fluoride, T is in Kelvin, and the parentheses indicate standard errors. REE2O3melt represents the summation of the melt REE concentrations for those REE which are compatible in the experimentally synthesized monazite (La-Sm and Gd). These experimental results suggest that the formation of monazite requires relatively high concentrations of P2O5 and Ce2O3 under crustal pressure and temperature conditions, making it challenging to crystallise directly from carbonatite melts. However, monazite may instead form through reactions involving evolved carbonatite melts, potentially interacting with siliceous wall rocks or replacing pre-existing phosphates like apatite, as has been observed in natural carbonatites.

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Publication Details

Journal
Geochimica et Cosmochimica Acta
Published
2025-02-04
DOI
https://doi.org/10.1016/j.gca.2025.01.039
Citations
3
Primary Topic
Geological and Geochemical Analysis
Type
article
Field-Weighted Citation Impact
5.60

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article

Monazite saturation in carbonatite melts at crustal and upper mantle conditions

Laura A. Miller, Gregory M. Yaxley, Andrew J. Berry, Srijita Ray
3 citations
Geochimica et Cosmochimica Acta
Geological and Geochemical Analysis
5.60
article

Monazite saturation in carbonatite melts at crustal and upper mantle conditions

Laura A. Miller, Gregory M. Yaxley, Andrew J. Berry, Srijita Ray
article en
3 citations

Abstract

Monazite (XPO4 where X = light rare earth element) is one of the most important ore minerals for rare earth elements (REE) mined from carbonatites. This study explores the influence of pressure, temperature and melt composition on the solubility of monazite in carbonate melt using piston cylinder experiments. We aim to understand how such a highly soluble phosphate mineral may sometimes crystallise from carbonatite magma and form economic deposits of REE. Our findings reveal that the solubility of monazite in a sodic-dolomitic carbonate melt is high over the entire pressure (1.0–2.0 GPa), temperature (1000-1450˚C), and compositional space (Na2O-CaO-MgO-SiO2-F) of our study. It increases from ∼ 26 to ∼ 61 wt% CePO4 equivalent over the temperature range of 1000–1450 °C at 2 GPa. However, the solubility product constant (lnKsp) decreases by approximately ∼ 23 % and 21 % equivalent with increasing melt SiO2 (from 0 to ∼ 18 wt% melt SiO2) at 1275 °C and fluoride (from 0 to ∼ 5 wt% melt F-) concentrations at 1100 °C respectively. Variations in melt Ca# (atomic Ca/(Mg + Ca) = 0.2–1.0) and pressure (1.0–2.0 GPa) have negligible impacts on monazite solubility. We use the experimental data to formulate an empirical model relating the solubility product constant (Ksp) of monazite in carbonate melt to temperature and melt compositional parameters: lnKsp=lnREE2O3melt.P2O5melt=1.310.50-[Formula presented]-3.35(0.34)×SiO2-1.68(0.34)×F where [] represents the mole fractions of oxides in the melt of the rare earth elements, phosphorus and silicon, and fluoride, T is in Kelvin, and the parentheses indicate standard errors. REE2O3melt represents the summation of the melt REE concentrations for those REE which are compatible in the experimentally synthesized monazite (La-Sm and Gd). These experimental results suggest that the formation of monazite requires relatively high concentrations of P2O5 and Ce2O3 under crustal pressure and temperature conditions, making it challenging to crystallise directly from carbonatite melts. However, monazite may instead form through reactions involving evolved carbonatite melts, potentially interacting with siliceous wall rocks or replacing pre-existing phosphates like apatite, as has been observed in natural carbonatites.

Geochimica et Cosmochimica ActaVol. 393
Diamond Light Source, Australian Government, Australian Research Council
Openalex Percentile: Top 6%
Geological and Geochemical Analysis
5.60
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