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A synthetic fluid inclusion study of the solubility of monazite-(La) and xenotime-(Y) in H2O-Na-K-Cl-F-CO2 fluids at 800 degrees C and 0.5 GPa TEXT SIZE: A A A
Alkali-rich F-Cl-CO2-bearing aqueous fluids are thought to be common ore-forming fluids of carbonatite-associated rare earth element (REE) deposits. Solubilities of synthetic monazite-(La) and xenotime-(Y) end-members in such fluids were determined at 800 degrees C and 0.5 GPa in a series of piston-cylinder experiments. At run conditions, solutions of NaCl/KCl (1.9 mol/kg) +/- CO2 (5% mole), NaCl/KCl (1.7 mol/kg) +/- NaF/KF (0.2 mol/kg) were trapped as synthetic fluid inclusions in quartz, and subsequently analyzed by laser ablation inductively coupled plasma mass spectrometry (LA-ICPMS). The resultant concentrations in these fluids are extremely low, ranging from 2.92 x 10(-6) to 3.05 x 10(-5) mol La/kg H2O and 3.97 x 10(-6) to 2.74 x 10(-5) mol Y/kg H2O. Such low solubilities indicate that fluids expelled from carbonatite melts contain insufficient phosphate and REE simultaneously to form REE deposits. Mixing REE-bearing fluids with phosphate-bearing aqueous fluids or interacting with apatite in the wall rock may be a key control on the deposition of REE phosphate minerals. In addition, our results show that, at nearly equal total ligand molality, solubilities of La and Y are both higher in F or CO2-bearing solutions than in Cl-only solutions, and the highest solubilities obtained overall were in NaCl + NaF solutions, which significantly increase by a factor of 9.4 for La and 6.1 for Y relative to NaCl-only solutions. Moreover, the solubility differences between xenotime and monazite in F/CO2-bearing solutions, shown as Y/La (molality ratio), are higher in K-bearing solutions than in Na-bearing solutions. Y/La in the NaCl + F/CO2 solutions are close to 1, whereas in the KCl + F/CO2 solutions Y/La increase to 2.9 and 2.0, respectively. These results indicate that during the evolution of carbonatitic fluids, enrichment of Na and F can significantly increase solubilities of all REE, whilst enrichment of K may promote the fractionation of HREE from LREE in the presence of F or CO2. (C) 2016 Elsevier B.V. All rights reserved.

Publication name

 CHEMICAL GEOLOGY, 442 121-129; 10.1016/j.chemgeo.2016.09.010 NOV 28 2016

Author(s)

 Zhou, Li; Mavrogenes, John; Spandler, Carl; Li, Heping

Corresponding author 

 ZHOU Li 
 zhouli_prc@hotmail.com
 1. Chinese Acad Sci, Inst Geochem, Key Lab High Temp & High Pressure Study Earths In, Guiyang 550002, Peoples R China
 2. Chinese Acad Sci, Inst Geochem, State Key Lab Ore Deposit Geochem, Guiyang 550002, Peoples R China
 3. Australian Natl Univ, Res Sch Earth Sci, Canberra, ACT 2601, Australia 

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