Monazite saturation in carbonatite melts at crustal and upper mantle conditions

Srijita Ray; Gregory M. Yaxley; Laura A. Miller; Andrew J. Berry

doi:10.1016/j.gca.2025.01.039

Monazite saturation in carbonatite melts at crustal and upper mantle conditions

Srijita Ray^*, Gregory M. Yaxley, Laura A. Miller, Andrew J. Berry

^*Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

2 Citations (Scopus)

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 (lnK_sp) 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 (K_sp) of monazite in carbonate melt to temperature and melt compositional parameters: lnK_sp=lnREE₂O₃_melt.P₂O₅_melt=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. REE₂O₃_melt 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.

Original language	English
Pages (from-to)	1-17
Number of pages	17
Journal	Geochimica et Cosmochimica Acta
Volume	393
DOIs	https://doi.org/10.1016/j.gca.2025.01.039
Publication status	Published - 15 Mar 2025

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@article{27d67a29d5a344268629185bff9f0a75,

title = "Monazite saturation in carbonatite melts at crustal and upper mantle conditions",

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.",

keywords = "Carbonatite, Critical Minerals, Experimental petrology, Monazite, Solubility",

author = "Srijita Ray and Yaxley, {Gregory M.} and Miller, {Laura A.} and Berry, {Andrew J.}",

note = "{\textcopyright} 2025 The Author(s). Published by Elsevier Ltd.",

year = "2025",

month = mar,

day = "15",

doi = "10.1016/j.gca.2025.01.039",

language = "English",

volume = "393",

pages = "1--17",

journal = "Geochimica et Cosmochimica Acta",

issn = "0016-7037",

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TY - JOUR

T1 - Monazite saturation in carbonatite melts at crustal and upper mantle conditions

AU - Ray, Srijita

AU - Yaxley, Gregory M.

AU - Miller, Laura A.

AU - Berry, Andrew J.

PY - 2025/3/15

Y1 - 2025/3/15

N2 - 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.

AB - 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.

KW - Carbonatite

KW - Critical Minerals

KW - Experimental petrology

KW - Monazite

KW - Solubility

UR - http://www.scopus.com/inward/record.url?scp=85217137523&partnerID=8YFLogxK

U2 - 10.1016/j.gca.2025.01.039

DO - 10.1016/j.gca.2025.01.039

M3 - Article

AN - SCOPUS:85217137523

SN - 0016-7037

VL - 393

SP - 1

EP - 17

JO - Geochimica et Cosmochimica Acta

JF - Geochimica et Cosmochimica Acta

ER -

Monazite saturation in carbonatite melts at crustal and upper mantle conditions

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