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ELECTROCHEMICAL COUPLE BEHAVIOR OF MANGANESE DIOXIDE WITH FERROUS/FERRIC IONS IN ACIDIC CHLORIDE MEDIUM

机译:酸性氯化物中二氧化锰与铁/铁离子的电化学偶合行为

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摘要

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_2 is due to the electrochemical couple reaction between MnO_2Mn~(2+) and Fe~(2+)/Fe~(3+) in the solution. The driving force for the process originates from the rest potential difference of the two couples. The reduction of MnO_2 is controlled by electrochemical kinetics, whereas the conversion of Fe~(2+) to Fe~(3+) is limited by diffusion. The factors such as the Mn~(2+), Fe~(2+), Fe~(3+), Cl~- 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:研究了二氧化锰与亚铁/铁离子在酸性氯化物介质中的电化学偶合行为。证明了MnO_2的溶解是由于溶液中MnO_2Mn〜(2+)与Fe〜(2 +)/ Fe〜(3+)之间的电化学偶合反应所致。该过程的驱动力源自两对夫妇的剩余电势差。 MnO_2的还原受电化学动力学控制,而Fe〜(2+)向Fe〜(3+)的转化受到扩散的限制。 Mn〜(2 +),Fe〜(2 +),Fe〜(3 +),Cl〜-浓度,溶液的pH值和温度等因素对偶联过程的动力学影响很大。这项研究将有助于阐明从深海中浸出锰结核和陆地上的二氧化锰矿石的机理。

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