4.5 Article

Leaching of WO3 from Sulfuric Acid Converted Product of Scheelite in NH3H2O-(NH4)2C2O4 Solution

Journal

JOURNAL OF SUSTAINABLE METALLURGY
Volume -, Issue -, Pages -

Publisher

SPRINGER
DOI: 10.1007/s40831-023-00750-w

Keywords

Tungstic acid; Calcium sulfate; Ammoniacal ammonium oxalate; Ammonium tungstate; Leaching mechanism

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This paper proposes a novel technology for tungsten extractive metallurgy, utilizing sulfuric acid conversion and ammonium salts leaching to efficiently extract WO3 from tungsten minerals. The optimized conditions were determined, resulting in a leaching efficiency of over 98%.
Due to the existence of large auxiliary material consumption, huge wastewater discharge, and high production cost in present tungsten extractive metallurgy practice, a novel technology featuring sulfuric acid conversion-ammonium salts leaching was proposed. Based on the complete conversion of tungsten minerals in sulfuric acid solution, this paper studied the leaching of WO3 from sulfuric acid converted product of scheelite in NH3H2O-(NH4)(2)C2O4 solution. The effect of leaching conditions on WO3 leaching efficiency and solid phase transformation was systemically investigated. The WO3 leaching efficiency was > 98% under optimized conditions of 1 mol/L (NH4)(2)C2O4, 3 mol/L NH3H2O, 350 rpm, 5 min, and 25 degrees C. The formed flaky CaC2O4H2O densely covered on the surface of banding or rodlike shaped CaSO4, which prevented the further transformation of CaSO4. The morphology of leaching residue was more irregular for converted product of scheelite concentrate than that for synthetic scheelite. Minor secondary reaction between CaSO4 and (NH4)(2)WO4 might occur with increased (NH4)(2)WO4 concentration, which could be restrained by the existence of (NH4)(2)C2O4 in solution due to the larger K-sp value of CaC2O4H2O than CaWO4. The leaching process could be explained by acid-base neutralization of H2WO4 and phase transformation of CaSO4 in NH3H2O-(NH4)(2)C2O4 solution.

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