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(106416)Electrochemical studies on dissolution and passivation behavior of low temperature bioleaching of chalcopyrite by Acidithiobacillus ferrivorans YL15

机译:(106416)酸酐硫吡啶铜矿低温生物浸润的溶解和钝化行为的电化学研究

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Bioleaching has been widely applied to recover metals from sulfide minerals at medium or high temperatures, however, little is known about the bioleaching at low temperature. Electrochemical analysis techniques such as cyclic voltammetry (CV), potentiodynamic polarization curve and electrochemical impedance spectroscopy (EIS), combined with surface detection methods such as scanning electron microscopy (SEM), applied to study the electrochemical behavior of chalcopyrite during bioleaching at 6 °C. Chalcopyrite bioleaching experiments demonstrated that the maximum cell density could achieve 5.3 × 10~8ells/mL. Copper extraction by Acidithiobacillus ferrivorans could reach 1.92 g/L, which is better than the 0.67 g/L of sterile experiment. CV tests found that as the leaching time passed, the anodic and cathodic current signals decreased and the anodic peak moved gradually from low potential to high potential. The increase of corrosion potential and the decrease of corrosion current in potentiodynamic polarization proved the passivation on the surface of the chalcopyrite. EIS results showed that ion exchange resistance increased from 306.1 Ω to 1913.0 Ω, which is larger than the passivation film impedance originated from elemental sulfur and polysulfide on the mineral surface. It suggested that the impedance of chalcopyrite electrode at low temperature is mainly due to ion exchange impedance but not passivation layer, which is different from the bioleaching at normal or high temperature.
机译:生物浸出已被广泛应用于回收来自培养基或高温下的硫化物矿物质的金属,然而,在低温下对生物浸出很少。电化学分析技术,如循环伏安法(CV),电位动力学偏振曲线和电化学阻抗光谱(EIS),与表面检测方法相结合,例如扫描电子显微镜(SEM),用于研究在6°C的生物浸料过程中硫代铜矿的电化学行为。黄铜矿生物浸入实验表明,最大细胞密度可以达到5.3×10〜8ell / ml。酸酐铁玻璃铜萃取可以达到1.92克/升,比无菌实验更好。 CV测试发现,随着浸出时间通过,阳极和阴极电流信号降低,阳极峰逐渐从低电位移动到高潜力。腐蚀电位的增加和电位变性极化中腐蚀电流的降低证明了硫代铜矿表面上的钝化。 EIS结果表明,离子交换电阻从306.1Ω增加到1913.0Ω,比矿物表面上的元素硫和多硫化物的钝化膜阻抗大。它表明,低温下的核黄素电极的阻抗主要是由于离子交换阻抗而不是钝化层,其与正常或高温下的生物浸出不同。

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