2014
DOI: 10.1016/j.electacta.2014.08.060
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Kinetics of Ferric Ion Reduction on Chalcopyrite and its Influence on Leaching up to 150 °C

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Cited by 31 publications
(10 citation statements)
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References 73 publications
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“…Furthermore, in direct contradiction to the theory proposed by Crundwell and co-workers,N icol showed that the generation of photocurrent during the oxidation of these minerals in acidic sulfate solutionswas relatedtothermal effects in the semiconductive surfacef ilm and not the bulk CuFeS 2 .D espite these contradictions about the mechanism of anodic dissolution of transition-metal sulfide minerals, there is al arge consensus on the formation of am etal-deficient-sulfide layer at the surface, which likely restricts mineral dissolution. [33][34][35][36] The energy generated at the surface of CuFeS 2 during oxidation by Fe 3 + ions in the presenceo fo xygen is lost as heat. [29][30][31][32] The literature provides good insight into the possible leaching of CuFeS 2 under oxidizing conditions or by reductive conversion of CuFeS 2 into Cu 2 S, which could then be oxidizedt o Cu 2 + .T he use of Fe 3 + ions in the presence of oxygen to leach Cu 2 + from CuFeS 2 has been rigorously studied in the past.…”
Section: Introductionmentioning
confidence: 99%
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“…Furthermore, in direct contradiction to the theory proposed by Crundwell and co-workers,N icol showed that the generation of photocurrent during the oxidation of these minerals in acidic sulfate solutionswas relatedtothermal effects in the semiconductive surfacef ilm and not the bulk CuFeS 2 .D espite these contradictions about the mechanism of anodic dissolution of transition-metal sulfide minerals, there is al arge consensus on the formation of am etal-deficient-sulfide layer at the surface, which likely restricts mineral dissolution. [33][34][35][36] The energy generated at the surface of CuFeS 2 during oxidation by Fe 3 + ions in the presenceo fo xygen is lost as heat. [29][30][31][32] The literature provides good insight into the possible leaching of CuFeS 2 under oxidizing conditions or by reductive conversion of CuFeS 2 into Cu 2 S, which could then be oxidizedt o Cu 2 + .T he use of Fe 3 + ions in the presence of oxygen to leach Cu 2 + from CuFeS 2 has been rigorously studied in the past.…”
Section: Introductionmentioning
confidence: 99%
“…[29][30][31][32] The literature provides good insight into the possible leaching of CuFeS 2 under oxidizing conditions or by reductive conversion of CuFeS 2 into Cu 2 S, which could then be oxidizedt o Cu 2 + .T he use of Fe 3 + ions in the presence of oxygen to leach Cu 2 + from CuFeS 2 has been rigorously studied in the past. [33][34][35][36] The energy generated at the surface of CuFeS 2 during oxidation by Fe 3 + ions in the presenceo fo xygen is lost as heat. In contrasttot he direct reduction of Fe 3 + on CuFeS 2 ,wepropose that the Fe 2 + /Fe 3 + redox reactionc ould proceed on as eparate electrode in ab attery-like cell setup.…”
Section: Introductionmentioning
confidence: 99%
“…Since Fe ion absorption is very small in spectroscopy, a colored complex is made of it that has a significant absorption in the UV-visible range compared to Fe ion and has high sensitivity in measuring iron ions. 29 Fig . 6 shows the UV-visible spectrum of 10 ml of the 0.001 molar Fe (III)-TPTZ, exposed to 0.01 g of (a) PAni, (b) PPy and (c) Poly(Ani-co-Py) for 30 min.…”
Section: Ferric Ion Reductionmentioning
confidence: 99%
“…The most often used lixiviants are acidic chloride media, acidic sulfate media and basic ammonia solutions, together with various oxidizing agents. [3][4][5][6][7] The most often used oxidizing agents are oxygen, ferric sulfate, ferric chloride or cupric chloride. [8][9][10][11][12][13] Various other oxidizing agents were investigated as well, such as hydrogen peroxide, ammonium persulfate, hypochlorite and ozone.…”
Section: Introductionmentioning
confidence: 99%