Electrochemical reduction of americium in acetonitrile medium
B. F. Myasoedov, Yu. M. Kulyako, I.S. Sklyarenko
Abstract
B. F. Myasoedov, Yu. M. Kulyako, I.S. Sklyarenko
Abstract
The electrochemical reduction of americium in acetonitrile medium was investigated. On the basis of the data obtained and a comparison of them with the results of a study of the mechanism of the reduction of rare-earth elements, it was suggested that americium is reduced through the divalent state. Unstable Am/sup 2 +/ cations are oxidized by the water contained in the solvent, with the formation of the hydrolyzed form of trivalent americium. The reduction of the latter ends in the liberation of a precipitate of a basic salt with composition Am(OH)/sub 2/./sub 6/(ClO/sub 4/)/sub 0/./sub 4/. The formal redox potential of the couple Am(III)/Am(II) in acetonitrile, equal to -1.55 V, was estimated.
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The electrochemical reduction of americium in acetonitrile medium was investigated. On the basis of the data obtained and a comparison of them with the results of a study of the mechanism of the reduction of rare-earth elements, it was suggested that americium is reduced through the divalent state. Unstable Am/sup 2 +/ cations are oxidized by the water contained in the solvent, with the formation of the hydrolyzed form of trivalent americium. The reduction of the latter ends in the liberation of a precipitate of a basic salt with composition Am(OH)/sub 2/./sub 6/(ClO/sub 4/)/sub 0/./sub 4/. The formal redox potential of the couple Am(III)/Am(II) in acetonitrile, equal to -1.55 V, was estimated.
Key concepts: Americium, Acetonitrile, Chemistry, Inorganic chemistry, Electrochemistry, Divalent, Cationic polymerization, Hydrolysis