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Electrochemical couple behavior of manganese dioxide with ferrous/ferric ions in acidic chloride medium

机译:二氧化锰具有碳酸氯/氯离子二氧化锰的电化学耦合行为

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The electrochemical couple behavior of manganese dioxide with ferrous ferric ions in acidic chloride medium was investigated. It was proven that the dissolution of MnO{sub}2 is due to the electrochemical couple reaction between MnO{sub}2/Mn{sup}(2+) and Fe{sup}(2+) Fe{sub}{sup}(3+) in the solution. The driving force for the process originates from the rest potential difference of the two couples. The reduction of MnO{sub}2 is controlled by electrochemical kinetics, whereas the conversion of Fe{sup}(2+) to Fe{sup}(3+) is limited by diffusion. The factors such as the Mn{sup}(2+), Fe{sup}(2+), Fe{sup}(3+), Cl{sup}- concentration, pH of the solution and the temperature. have much influence on the kinetics of the couple process. This study will be useful to elucidate the mechanism for the leaching of manganese nodule from the deep ocean as well as manganese dioxide ores in land.
机译:研究了二氧化锰具有亚铁氯化亚铁离子的二氧化锰的电化学耦合行为。据证明,MnO {sub} 2的溶解是由于MnO {sub} 2 / mn {sup}(2+)和fe {sup}(2+)fe {sub}} {sup}之间的电化学耦合反应是导致的(3+)在解决方案中。该过程的驱动力源自两对夫妻的剩余势差。 MnO {Sub} 2的还原由电化学动力学控制,而Fe {sup}(2+)转化为Fe {sup}(3+)的转化通过扩散限制。诸如Mn {sup}(2+),fe {sup}(2+),fe {sup}(3+),cl {sup} - 浓度,溶液的pH和温度的因素。对夫妻过程的动力学有很大影响。本研究将有助于阐明从深海和土地中的二氧化锰矿石浸出锰结节的机制。

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