The present invention is directed to a method for the separation of an actinide from another metal. The method comprises the following steps: (a) establishing a non-homogeneous magnetic field across a separation column containing a paramagnetic packing material and (b) providing a fluid containing the actinide and the another metal to the separation column wherein the fluid and the paramagnetic packing material are exposed to the non-homogeneous magnetic field. The non-homogeneous magnetic field is produced by a magnet having a first pole for magnetic interaction with a second pole of the magnet wherein the first pole has a different surface area than the second pole. The non-homogeneous magnetic field has a magnetic field gradient of about 500 lines/cm.sup.2/cm or more. In addition, the present invention is also directed to a method for the separation of one heavy metal from another heavy metal.

Novel dissymmetric N,N-dialkylamides which meet the following formula (I): ##STR00001##
where R represents a linear or branched alkyl group at C.sub.8 to C.sub.15. A method for synthesizing these N,N-dialkylamides, and to the uses of same as extractants, alone or in admixture, in order to extract uranium and/or plutonium from an aqueous acid solution, or to totally or separate uranium from plutonium from an aqueous acid solution and, in particular, an aqueous solution resulting from dissolving spent nuclear fuel in nitric acid. Further, a method for processing an aqueous solution resulting from the dissolution of a spent nuclear fuel in nitric acid, allowing the uranium and plutonium contained in the solution to be extracted, separated and decontaminated in a single cycle, without requiring any plutonium reduction operation, and in which one of the aforementioned N,N-dialkylamides or a mixture of same is used as extractant. Applications for the method include the processing of spent nuclear fuels, in particular comprising uranium (e.g. UOX) or uranium and plutonium (e.g. MOX).

Novel dissymmetric N,N-dialkylamides which meet the following formula (I): ##STR00001##
where R represents a linear or branched alkyl group at C.sub.8 to C.sub.15. A method for synthesizing these N,N-dialkylamides, and to the uses of same as extractants, alone or in admixture, in order to extract uranium and/or plutonium from an aqueous acid solution, or to totally or separate uranium from plutonium from an aqueous acid solution and, in particular, an aqueous solution resulting from dissolving spent nuclear fuel in nitric acid. Further, a method for processing an aqueous solution resulting from the dissolution of a spent nuclear fuel in nitric acid, allowing the uranium and plutonium contained in the solution to be extracted, separated and decontaminated in a single cycle, without requiring any plutonium reduction operation, and in which one of the aforementioned N,N-dialkylamides or a mixture of same is used as extractant. Applications for the method include the processing of spent nuclear fuels, in particular comprising uranium (e.g. UOX) or uranium and plutonium (e.g. MOX).

A method for processing a spent nuclear fuel is disclosed which includes a step for decontaminating uranium(VI) from one or more actinides(IV) and more specially from neptunium and/or plutonium, by complexing this (these) actinide(s)(IV). This method includes a step for decontaminating uranium (VI) from at least one actinide(IV), which decontaminating step comprises at least one operation for stripping the actinide(IV) from an organic phase, not miscible with water, and wherein uranium(VI) and the actinide(IV) are present, by putting the organic phase into contact with an aqueous phase comprising nitric acid and at least one complexing agent which more strongly complexes actinides(IV) than uranium(VI), and then separating the organic phase from the nitric aqueous phase, wherein the at least one complexing agent is a diglycolamide.

A method for processing a spent nuclear fuel is disclosed which includes a step for decontaminating uranium(VI) from one or more actinides(IV) and more specially from neptunium and/or plutonium, by complexing this (these) actinide(s)(IV). This method includes a step for decontaminating uranium (VI) from at least one actinide(IV), which decontaminating step comprises at least one operation for stripping the actinide(IV) from an organic phase, not miscible with water, and wherein uranium(VI) and the actinide(IV) are present, by putting the organic phase into contact with an aqueous phase comprising nitric acid and at least one complexing agent which more strongly complexes actinides(IV) than uranium(VI), and then separating the organic phase from the nitric aqueous phase, wherein the at least one complexing agent is a diglycolamide.

Reactor target assemblies are provided that can include a housing defining a perimeter of at least one volume and Np or Am spheres within the one volume. Reactor assemblies are provided that can include a reactor vessel and a bundle of target assemblies within the reactor vessel, at least one of the target assemblies comprising a housing defining a volume with Np or Am spheres being within the volume. Irradiation methods are also provided that can include irradiating Np or Am spheres within a nuclear reactor, then removing the irradiated spheres from the reactor and treating the irradiated spheres.

Novel dissymmetric N,N-dialkylamides which meet the following formula (I):

##STR00001##

where R represents a linear or branched alkyl group at C.sub.8 to C.sub.15. A method for synthesizing these N,N-dialkylamides, and to the uses of same as extractants, alone or in admixture, in order to extract uranium and/or plutonium from an aqueous acid solution, or to totally or separate uranium from plutonium from an aqueous acid solution and, in particular, an aqueous solution resulting from dissolving spent nuclear fuel in nitric acid. Further, a method for processing an aqueous solution resulting from the dissolution of a spent nuclear fuel in nitric acid, allowing the uranium and plutonium contained in the solution to be extracted, separated and decontaminated in a single cycle, without requiring any plutonium reduction operation, and in which one of the aforementioned N,N-dialkylamides or a mixture of same is used as extractant. Applications for the method include the processing of spent nuclear fuels, in particular comprising uranium (e.g. UOX) or uranium and plutonium (e.g. MOX).

Novel dissymmetric N,N-dialkylamides which meet the following formula (I):

##STR00001##

where R represents a linear or branched alkyl group at C.sub.8 to C.sub.15. A method for synthesizing these N,N-dialkylamides, and to the uses of same as extractants, alone or in admixture, in order to extract uranium and/or plutonium from an aqueous acid solution, or to totally or separate uranium from plutonium from an aqueous acid solution and, in particular, an aqueous solution resulting from dissolving spent nuclear fuel in nitric acid. Further, a method for processing an aqueous solution resulting from the dissolution of a spent nuclear fuel in nitric acid, allowing the uranium and plutonium contained in the solution to be extracted, separated and decontaminated in a single cycle, without requiring any plutonium reduction operation, and in which one of the aforementioned N,N-dialkylamides or a mixture of same is used as extractant. Applications for the method include the processing of spent nuclear fuels, in particular comprising uranium (e.g. UOX) or uranium and plutonium (e.g. MOX).

Uses of cyclic amine monoamides for extracting uranium(VI) and/or plutonium(IV) from an acidic aqueous solution, as well as for totally or partially separating uranium(VI) from plutonium(IV) from an acidic aqueous solution. A method for treating an aqueous solution resulting from the dissolution of spent nuclear fuel in nitric acid to extract, separate and decontaminate uranium(VI) and plutonium(IV) in a single cycle and without resorting to any operation of reducing plutonium(IV), and wherein a cyclic amine monoamide or a mixture of cyclic amine monoamides is used as extractant. The cyclic amine monoamides have formula (I):

##STR00001##

Uses of cyclic amine monoamides for extracting uranium(VI) and/or plutonium(IV) from an acidic aqueous solution, as well as for totally or partially separating uranium(VI) from plutonium(IV) from an acidic aqueous solution. A method for treating an aqueous solution resulting from the dissolution of spent nuclear fuel in nitric acid to extract, separate and decontaminate uranium(VI) and plutonium(IV) in a single cycle and without resorting to any operation of reducing plutonium(IV), and wherein a cyclic amine monoamide or a mixture of cyclic amine monoamides is used as extractant. The cyclic amine monoamides have formula (I):

##STR00001##