This work presents a study of the electrochemical properties of Th chloride ions dissolved in a molten LiCl–KCl eutectic, in a temperature range of 693–823 K. Transient electrochemical techniques such as cyclic voltammetry, chronopotentiommetry and chronoamperometry have been used in order to investigate the reduction mechanism on a tungsten electrode and the diffusion coefficient of dissolved Th ions. All techniques showed that only one valence state was stable in the melt. The reduction into Th metal was found to occur according to a onestep mechanism, through a nucleation-controlled process which requires an overpotential of several 100mV. At 723 K, the diffusion coefficient is DTh(723 K) = 3.15±0.15×10−5 cm2 s−1. EMF measurements indicated that, at 723 K, the standard apparent potential isE0 ThCl4/Th (723 K) =−2.582V versus Cl2/Cl−, and the activity coefficient γThCl4 (723 K) = 4.6×10−4 on the mole fraction scale (based on a pure liquid reference state).

CASSAYRE Laurent;  SERP Jerome;  SOUCEK Pavel;  MALMBECK Rikard;  REBIZANT Jean;  GLATZ Jean-Paul; 

2007-08-13

PERGAMON-ELSEVIER SCIENCE LTD

JRC38167

https://publications.jrc.ec.europa.eu/repository/handle/JRC38167,