Abstract <p>This study investigated the kinetics of tellurium leaching from copper anode slime in a manganese dioxide–sulfuric acid system. The results revealed that the tellurium leaching proceeded in two stages. The activation energy for the initial stage was 104.34&#xa0;kJ/mol, indicating that this stage was predominantly controlled by chemical reactions. The reaction order of MnO<sub>2</sub> and H<sub>2</sub>SO<sub>4</sub> in this stage were determined to be 0.33 and 0.26, respectively, reflecting that the leaching rate was influenced by both reactants. In the second stage, the activation energy decreased to 32.51&#xa0;kJ/mol, suggesting a mixed control mechanism involving both chemical reaction and diffusion. The reaction order of MnO<sub>2</sub> declined to 0.043, indicating a diminished influence of MnO<sub>2</sub> concentration on the leaching rate, whereas the reaction order of H<sub>2</sub>SO<sub>4</sub> increased to 1.74, underscoring the critical role of acid concentration. Under strongly acidic conditions, Mn(IV) species released from MnO<sub>2</sub> oxidized tellurium in both Ag<sub>2</sub>Te and elemental Te. Under optimized parameters, the extraction of tellurium reached 96.35%. Furthermore, increasing the temperature and applying controlled stirring conditions enhanced the diffusion of Mn(IV) and significantly improved leaching efficiency.</p> Graphical Abstract <p></p>

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Leaching Kinetics of Tellurium from Copper Anode Slime Using a Manganese Dioxide–Sulfuric Acid System

  • Junpeng Wang,
  • Bo Liu,
  • Yuyuan Zhang

摘要

Abstract

This study investigated the kinetics of tellurium leaching from copper anode slime in a manganese dioxide–sulfuric acid system. The results revealed that the tellurium leaching proceeded in two stages. The activation energy for the initial stage was 104.34 kJ/mol, indicating that this stage was predominantly controlled by chemical reactions. The reaction order of MnO2 and H2SO4 in this stage were determined to be 0.33 and 0.26, respectively, reflecting that the leaching rate was influenced by both reactants. In the second stage, the activation energy decreased to 32.51 kJ/mol, suggesting a mixed control mechanism involving both chemical reaction and diffusion. The reaction order of MnO2 declined to 0.043, indicating a diminished influence of MnO2 concentration on the leaching rate, whereas the reaction order of H2SO4 increased to 1.74, underscoring the critical role of acid concentration. Under strongly acidic conditions, Mn(IV) species released from MnO2 oxidized tellurium in both Ag2Te and elemental Te. Under optimized parameters, the extraction of tellurium reached 96.35%. Furthermore, increasing the temperature and applying controlled stirring conditions enhanced the diffusion of Mn(IV) and significantly improved leaching efficiency.

Graphical Abstract