The invention provides an automated method for isolating a targeted isotope, the method having the steps of supplying a dissolved uranium targets into a first reaction environment; precipitating non-targeted isotope within the first reaction environment transferring liquid phase targeted isotope to a second reaction environment; precipitating the liquid phase targeted isotope in the second reaction environment; dissolving the precipitated targeted isotope; transferring the dissolved targeted isotope to a third reaction environment; and precipitating non-targeted isotope (i.e., iodine), such that the targeted isotope remains in the solution. Also provided is an automated system for isolating isotopes, the system having a plurality of reaction environments adapted to pneumatically receive and disgorge reactants and products via remotely actuated valves positioned between each of the reaction environments.

The invention provides an automated method for isolating a targeted isotope, the method having the steps of supplying a dissolved uranium targets into a first reaction environment; precipitating non-targeted isotope within the first reaction environment transferring liquid phase targeted isotope to a second reaction environment; precipitating the liquid phase targeted isotope in the second reaction environment; dissolving the precipitated targeted isotope; transferring the dissolved targeted isotope to a third reaction environment; and precipitating non-targeted isotope (i.e., iodine), such that the targeted isotope remains in the solution. Also provided is an automated system for isolating isotopes, the system having a plurality of reaction environments adapted to pneumatically receive and disgorge reactants and products via remotely actuated valves positioned between each of the reaction environments.

A process of extracting metals from a wet mass includes a step A of concentrating the metals in a carbonaceous solid with a thermochemical treatment of the wet mass, with the ancillary production of a treatment gas; a step B of thermochemical decomposition of the carbonaceous solid in an atmosphere constituted by an operating gas which contains oxygen in substoichiometric quantity to carry out the thermochemical decomposition in order to promote a combination of the metals with substances present in the carbonaceous solid to form salts and others solid compounds and to concentrate the latter in residual ashes of the carbonaceous solid at the same time providing for the formation of a combustible synthesis gas comprising hydrocarbons from the carbonaceous solid; and a step C of extraction of the metals from the ashes produced.