Thermodynamic analysis of the decomposition of scheelite by oxalic acid

The equilibrium diagram of the Ca-W-Oa-H<sub>2</sub>O system for the H<sub>2</sub>C<sub>2</sub>O<sub>4</sub> leaching of scheelite at 298 K was constructed. This diagram clarifies the dominant regions of each component in the system as well as the variation rules of key components with pH value and total concentration of free H<sub>2</sub>C<sub>2</sub>O<sub>4</sub>, thereby confirming the thermodynamic conditions for the H<sub>2</sub>C<sub>2</sub>O<sub>4</sub> leaching of scheelite. Theoretical analysis results indicate that H<sub>2</sub>C<sub>2</sub>O<sub>4</sub> can effectively leach scheelite, and the concentration of H<sub>2</sub>C<sub>2</sub>O<sub>4</sub> is a crucial factor influencing the leaching efficiency. When 1 < pH < 6.4, scheelite reacts with H<sub>2</sub>C<sub>2</sub>O<sub>4</sub> to form precipitates of H<sub>2</sub>WO<sub>4(s)</sub> and CaC<sub>2</sub>O<sub>4(s)</sub>. Under the condition of maintaining a high concentration of free H<sub>2</sub>C<sub>2</sub>O<sub>4(aq)</sub>, H<sub>2</sub>WO<sub>4(s)</sub> further reacts with H<sub>2</sub>C<sub>2</sub>O<sub>4(aq)</sub>, and the formation of H<sub>2</sub>[WO<sub>3</sub>(C<sub>2</sub>O<sub>4</sub>·H<sub>2</sub>O)] with high solubility is predicted, which promotes the leaching of scheelite. When 6.4 < pH < 14.6, the ionization of H<sub>2</sub>C<sub>2</sub>O<sub>4</sub> is enhanced with the increase of pH, leading to the rise in the concentrations of C<sub>2</sub>O<sub>4</sub> <sup>2-</sup> and WO<sub>4</sub> <sup>2-</sup>. When pH > 14.6, the binding effect between OH<sup>-</sup> and Ca<sup>2+</sup> in the system is sharply strengthened, and CaC<sub>2</sub>O<sub>4(s)</sub> is gradually converted into Ca(OH)<sub>2(s)</sub>. Based on the thermodynamic analysis results, experimental verification of H<sub>2</sub>C<sub>2</sub>O<sub>4</sub> leaching of scheelite was carried out. Under the optimal conditions of H<sub>2</sub>C<sub>2</sub>O<sub>4</sub> concentration of 2.2 mol L<sup>-1</sup>, reaction temperature of 80 °C, reaction time of 5 h, liquid-to-solid ratio of 15 : 1, and stirring speed of 100 rpm, the leaching rate of WO<sub>3</sub> reached 99.54%, with only 0.53% of WO<sub>3</sub> remaining in the leaching residue. Comparison of the XRD, EDS, and FTIR characterization results of raw scheelite and oxalic acid-leached residue reveals that during the leaching process, most of the tungsten enters the leachate in a highly soluble form, while calcium combines with C<sub>2</sub>O<sub>4</sub> <sup>2-</sup> to form CaC<sub>2</sub>O<sub>4</sub>·H<sub>2</sub>O precipitate, which is retained in the leaching residue.

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Publication Details

Journal
RSC Advances
Published
2026-01-01
DOI
https://doi.org/10.1039/d6ra01141a
Primary Topic
Molten salt chemistry and electrochemical processes
Type
article
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article

Thermodynamic analysis of the decomposition of scheelite by oxalic acid

RSC Advances
Molten salt chemistry and electrochemical processes
article

Thermodynamic analysis of the decomposition of scheelite by oxalic acid

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Abstract

The equilibrium diagram of the Ca-W-Oa-H<sub>2</sub>O system for the H<sub>2</sub>C<sub>2</sub>O<sub>4</sub> leaching of scheelite at 298 K was constructed. This diagram clarifies the dominant regions of each component in the system as well as the variation rules of key components with pH value and total concentration of free H<sub>2</sub>C<sub>2</sub>O<sub>4</sub>, thereby confirming the thermodynamic conditions for the H<sub>2</sub>C<sub>2</sub>O<sub>4</sub> leaching of scheelite. Theoretical analysis results indicate that H<sub>2</sub>C<sub>2</sub>O<sub>4</sub> can effectively leach scheelite, and the concentration of H<sub>2</sub>C<sub>2</sub>O<sub>4</sub> is a crucial factor influencing the leaching efficiency. When 1 < pH < 6.4, scheelite reacts with H<sub>2</sub>C<sub>2</sub>O<sub>4</sub> to form precipitates of H<sub>2</sub>WO<sub>4(s)</sub> and CaC<sub>2</sub>O<sub>4(s)</sub>. Under the condition of maintaining a high concentration of free H<sub>2</sub>C<sub>2</sub>O<sub>4(aq)</sub>, H<sub>2</sub>WO<sub>4(s)</sub> further reacts with H<sub>2</sub>C<sub>2</sub>O<sub>4(aq)</sub>, and the formation of H<sub>2</sub>[WO<sub>3</sub>(C<sub>2</sub>O<sub>4</sub>·H<sub>2</sub>O)] with high solubility is predicted, which promotes the leaching of scheelite. When 6.4 < pH < 14.6, the ionization of H<sub>2</sub>C<sub>2</sub>O<sub>4</sub> is enhanced with the increase of pH, leading to the rise in the concentrations of C<sub>2</sub>O<sub>4</sub> <sup>2-</sup> and WO<sub>4</sub> <sup>2-</sup>. When pH > 14.6, the binding effect between OH<sup>-</sup> and Ca<sup>2+</sup> in the system is sharply strengthened, and CaC<sub>2</sub>O<sub>4(s)</sub> is gradually converted into Ca(OH)<sub>2(s)</sub>. Based on the thermodynamic analysis results, experimental verification of H<sub>2</sub>C<sub>2</sub>O<sub>4</sub> leaching of scheelite was carried out. Under the optimal conditions of H<sub>2</sub>C<sub>2</sub>O<sub>4</sub> concentration of 2.2 mol L<sup>-1</sup>, reaction temperature of 80 °C, reaction time of 5 h, liquid-to-solid ratio of 15 : 1, and stirring speed of 100 rpm, the leaching rate of WO<sub>3</sub> reached 99.54%, with only 0.53% of WO<sub>3</sub> remaining in the leaching residue. Comparison of the XRD, EDS, and FTIR characterization results of raw scheelite and oxalic acid-leached residue reveals that during the leaching process, most of the tungsten enters the leachate in a highly soluble form, while calcium combines with C<sub>2</sub>O<sub>4</sub> <sup>2-</sup> to form CaC<sub>2</sub>O<sub>4</sub>·H<sub>2</sub>O precipitate, which is retained in the leaching residue.

RSC AdvancesVol. 16(18)
Ganzhou People's Hospital (CN), Xiamen Tungsten (China) (CN), Jiangxi College of Applied Technology (CN), Jiangxi University of Science and Technology (CN)
Openalex Percentile: Top 11%
Molten salt chemistry and electrochemical processes
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