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首页> 外文期刊>Minerals Engineering >Simulating the main stages of chalcopyrite leaching and bioleaching in ferrous ions solution: An electrochemical impedance study with a modified carbon paste electrode
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Simulating the main stages of chalcopyrite leaching and bioleaching in ferrous ions solution: An electrochemical impedance study with a modified carbon paste electrode

机译:含铁离子溶液浸出和生物浸出的主要阶段溶液:用改性碳浆料电极进行电化学阻抗研究

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In this work, we present an electrochemical study using a carbon paste electrode modified with chalcopyrite (CuFeS2) in solution A of T&K medium with different ferrous ion concentrations, in the absence and presence of the bacterium Acidithiobacillus ferrooxidans. The aim was to evaluate the influence of ferrous ions and bacteria on the electrochemical behavior of chalcopyrite. Electrochemical impedance spectroscopy (EIS) was used to investigate the processes occurring at the electrode/solution interface in the different systems, considering the charge transfer reactions involving chalcopyrite and ferrous ions, the presence of a multicomponent layer, and diffusion. The main changes in the chalcopyrite response occurred before 67 h or 43 h of immersion, in the absence or presence of ferrous ions, respectively, indicating that the surface oxide layer present on chalcopyrite was dissolved faster in the presence of ferrous ions. The addition of bacteria decreased the charge transfer reaction resistance, especially when ferrous ions were present. In the presence of Fe2+, sulfur and jarosite were detected in the solid residues after leaching, while only jarosite was detected in the bioleaching experiment. The results suggested that ferrous ions accelerated the dissolution of chalcopyrite, and that overlayers including biofilms did not halt chalcopyrite dissolution, indicating that there was no passivation. (C) 2016 Elsevier Ltd. All rights reserved.
机译:在这项工作中,我们使用用不同亚铁浓度的T&K培养基中用含核培养基(Cufes2)修饰的碳糊电极的电化学研究,在没有酸酐酸胆胆硼磷脂的情况下的情况下。目的是评估铁离子和细菌对硫代铜矿电化学行为的影响。使用电化学阻抗光谱(EIS)用于研究在不同系统中的电极/溶液界面中发生的方法,考虑涉及含氯铜矿和铁离子的电荷转移反应,是多组分层的存在和扩散。在浸渍的67小时或43小时之前,分别在浸渍的67小时或43小时之前发生的主要变化,其分别在亚铁离子的情况下,表明在铁壳上存在的表面氧化物层在亚铁离子存在下溶解。细菌的添加降低了电荷转移反应性,尤其是当存在亚铁离子时。在浸出后在固体残基中检测硫和jar,而在生物浸入实验中检测到硫磺和jar。结果表明,黑色离子加速了硫代铜矿的溶解,并且包括生物膜的覆盖物没有停止硫代铜矿溶解,表明没有钝化。 (c)2016 Elsevier Ltd.保留所有权利。

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