The present invention relates to a method for recovering plutonium from spent radioactive fuel. In one embodiment, the method comprises steps of extracting tetravalent plutonium from an aqueous solution of the spent radioactive fuel using a first organic solvent comprising tributyl phosphate; reducing tetravalent plutonium to trivalent plutonium by adding to an organic phase a second organic solvent comprising dimethylhydroxylamine; and stripping plutonium into the aqueous phase for recycling by adding an aqueous dilute acid solution into an organic phase. The method can significantly improve the efficiency of recovering plutonium from spent radioactive fuel compared with HAN stripping, and at the same time, can avoid the problems resulting from U(IV) reduction and extraction.

A dissymmetric RN,N-dialkylamides of formula (I) in which: R.sup.1 represents a linear C.sub.1 to C.sub.4 alkyl, R.sup.2 represents a linear C.sub.1 to C.sub.10 alkyl, and R.sup.3 represents a linear or branched C.sub.6 to C.sub.15 alkyl, where R.sup.3 is different from a n-octyl, n-decyl, n-dodecyl, 2-ethylhexyl and 2-ethyloctyl group when R.sup.1 represents a n-butyl group and R.sup.2 represents an ethyl group. A method for synthesising the N,N-dialkylamides, and uses of same for extracting uranium and/or plutonium from an aqueous acid solution or for fully or partially separating the uranium from the plutonium contained in an aqueous acid solution and a solution resulting from the dissolution of spent nuclear fuel in nitric acid. A method for treating an aqueous solution resulting from the dissolution of spent nuclear fuel in nitric acid, which allows the uranium and the plutonium contained in the solution to be extracted, separated and decontaminated in a single cycle.

A dissymmetric RN,N-dialkylamides of formula (I) in which: R.sup.1 represents a linear C.sub.1 to C.sub.4 alkyl, R.sup.2 represents a linear C.sub.1 to C.sub.10 alkyl, and R.sup.3 represents a linear or branched C.sub.6 to C.sub.15 alkyl, where R.sup.3 is different from a n-octyl, n-decyl, n-dodecyl, 2-ethylhexyl and 2-ethyloctyl group when R.sup.1 represents a n-butyl group and R.sup.2 represents an ethyl group. A method for synthesising the N,N-dialkylamides, and uses of same for extracting uranium and/or plutonium from an aqueous acid solution or for fully or partially separating the uranium from the plutonium contained in an aqueous acid solution and a solution resulting from the dissolution of spent nuclear fuel in nitric acid. A method for treating an aqueous solution resulting from the dissolution of spent nuclear fuel in nitric acid, which allows the uranium and the plutonium contained in the solution to be extracted, separated and decontaminated in a single cycle.

A method of producing uranium halides is disclosed in which chlorine gas is introduced into a liquid uranium-nickel alloy. NaCl salt is surrounding the crucible containing the liquid uranium-nickel alloy, producing a eutectic mixture of NaCl—UCl.sub.3. Upon chlorination, the metal halide dissolves in the matrix salt forming a solution. Adding the reactant metal, uranium to the nickel, the alloy is able to remain molten throughout processing. The liquid metal alloy may be removed from the salt bath, while the halogen gas continues to enter the system through the sparge until the desired composition of NaCl—UCl.sub.3—UCl.sub.4 is achieved. The method and system can be used to produce other metal halide salts such as actinide, lanthanide or transition metal halides contained in a matrix salt consisting of alkali and/or alkaline earth halides.

A method of producing uranium halides is disclosed in which chlorine gas is introduced into a liquid uranium-nickel alloy. NaCl salt is surrounding the crucible containing the liquid uranium-nickel alloy, producing a eutectic mixture of NaCl—UCl.sub.3. Upon chlorination, the metal halide dissolves in the matrix salt forming a solution. Adding the reactant metal, uranium to the nickel, the alloy is able to remain molten throughout processing. The liquid metal alloy may be removed from the salt bath, while the halogen gas continues to enter the system through the sparge until the desired composition of NaCl—UCl.sub.3—UCl.sub.4 is achieved. The method and system can be used to produce other metal halide salts such as actinide, lanthanide or transition metal halides contained in a matrix salt consisting of alkali and/or alkaline earth halides.

A method for preparing a powder comprising an intimate mixture of U.sub.3O.sub.8 particles and PuO.sub.2 particles and which may further comprise particles of ThO.sub.2 or NpO.sub.2. The method comprises: preparing, via oxalic precipitations, an aqueous suspension S.sub.1 of particles of uranium(IV) oxalate and an aqueous suspension S.sub.2 of particles of plutonium(IV) oxalate; mixing the aqueous suspension S.sub.1 with the aqueous suspension S.sub.2 to obtain an aqueous suspension S.sub.1+2, separating the aqueous suspension S.sub.1+2 into an aqueous phase and a solid phase comprising the particles of uranium(IV) oxalate and the particles of plutonium(IV) oxalate; and calcining the solid phase to convert (1) the particles of uranium(IV) oxalate to particles of triuranium octoxide and (2) the particles of plutonium(IV) oxalate to particles of plutonium(IV) dioxide, whereby the powder is obtained.

A method for preparing a powder comprising an intimate mixture of U.sub.3O.sub.8 particles and PuO.sub.2 particles and which may further comprise particles of ThO.sub.2 or NpO.sub.2. The method comprises: preparing, via oxalic precipitations, an aqueous suspension S.sub.1 of particles of uranium(IV) oxalate and an aqueous suspension S.sub.2 of particles of plutonium(IV) oxalate; mixing the aqueous suspension S.sub.1 with the aqueous suspension S.sub.2 to obtain an aqueous suspension S.sub.1+2, separating the aqueous suspension S.sub.1+2 into an aqueous phase and a solid phase comprising the particles of uranium(IV) oxalate and the particles of plutonium(IV) oxalate; and calcining the solid phase to convert (1) the particles of uranium(IV) oxalate to particles of triuranium octoxide and (2) the particles of plutonium(IV) oxalate to particles of plutonium(IV) dioxide, whereby the powder is obtained.

The present disclosure provides systems and methods for thermal molten salt reactor fuel-salt preparation. In one implementation, the method may comprise providing fuel assemblies having fuel pellets, removing the fuel pellets and spent fuel pieces from the fuel assemblies, processing the spent fuel pellets and fuel pieces into a fluoride salt by ultimate oxidation, reduction, and fluorination of uranium and its associated fuel constituents, and filtering water vapor formed during the reduction and fluorination operations.

The present disclosure provides systems and methods for thermal molten salt reactor fuel-salt preparation. In one implementation, the method may comprise providing fuel assemblies having fuel pellets, removing the fuel pellets and spent fuel pieces from the fuel assemblies, processing the spent fuel pellets and fuel pieces into a fluoride salt by ultimate oxidation, reduction, and fluorination of uranium and its associated fuel constituents, and filtering water vapor formed during the reduction and fluorination operations.

A process for dissolving nuclear fuel, in particular irradiated nuclear fuel, comprising immersion of the nuclear fuel in a nitric acid solution. This dissolution process further comprises mechanical milling of the nuclear fuel, this mechanical milling being performed in the nitric acid solution during the immersion. The disclosure also relates to the use of a mill equipped with mechanical milling structure to implement the dissolution process.