Method for processing spent nuclear fuel comprising a step for decontaminating uranium (VI) from at least one actinide (IV) by complexing this actinide (IV)

Patent metadata

Field	Value
Publication number	US-10210958-B2
Application number	US-201415104154-A
Country	US
Kind code	B2
Filing date	Dec 18, 2014
Priority date	Dec 20, 2013
Publication date	Feb 19, 2019
Grant date	Feb 19, 2019

Abstract

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.

First claim

The invention claimed is:

1. A method for processing a spent nuclear fuel, which comprises a decontamination of uranium(VI) from an actinide(IV), the decontamination comprising at least a stripping of the actinide(IV) from an organic phase, which is not miscible with water and which comprises uranium(VI) and the actinide(IV), the stripping comprising putting the organic phase in 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 aqueous phase, the complexing agent being a diglycolamide.

2. The method of claim 1 , wherein the diglycolamide is N,N,N′,N′-tetramethyldiglycolamide, N,N,N′,N′-tetraethyldiglycolamide, N,N,N′,N′-tetrapropyldiglycolamide, N,N-dipropyldiglycolamic acid, or mixtures thereof.

3. The method of claim 2 , wherein the diglycolamide is N,N,N′,N′-tetraethyldiglycolamide.

4. The method of claim 1 , wherein the aqueous phase comprises from 0.01 mol/L to 0.1 mol/L of diglycolamide.

5. The method of claim 1 , wherein the aqueous phase comprises from 0.2 mol/L to 3 mol/L of nitric acid.

6. The method of claim 1 , wherein the decontamination of uranium(VI) from the actinide(IV) further comprises a washing of the aqueous phase stemming from the stripping of the actinide(IV), the washing comprising putting the aqueous phase in contact with an organic phase comprising an extractant of uranium(VI), and then separating the organic phase from the aqueous phase.

7. The method of claim 6 , wherein the extractant is tri-n-butyl phosphate.

8. The method of claim 1 , wherein the actinide(IV) is neptunium(IV), plutonium(IV), thorium(IV), or mixtures thereof.

9. The method of claim 1 , wherein the decontamination of uranium(VI) from the actinide(IV) is a decontamination of uranium(VI) from neptunium(IV).

10. The method of claim 9 , comprising:
a) a treatment of a first aqueous phase resulting from a dissolution of a spent nuclear fuel in nitric acid and comprising uranium(VI), plutonium(IV), neptunium(VI), actinides(III) and fission products, to decontaminate uranium(VI), plutonium(IV) and neptunium(VI) from the actinides(III) and the fission products, the treatment comprising:
a 1 ) a co-extraction of uranium(VI), plutonium(IV) and neptunium(VI) from the first aqueous phase, the co-extraction comprising putting the first aqueous phase in contact with an organic phase comprising tri-n-butyl phosphate in an organic diluent, and then separating the organic phase from the first aqueous phase; and
a 2 ) a washing of the organic phase from a 1 ), the washing comprising putting the organic phase into contact with a second aqueous phase comprising nitric acid, and then separating the organic phase from the second aqueous phase; whereby a first organic phase is obtained, which comprises uranium(VI), plutonium(IV) and neptunium(VI);

b) a partition of the uranium and the plutonium present in the first organic phase into two aqueous solutions, a first aqueous solution comprising plutonium decontaminated from uranium and neptunium, and a second aqueous solution comprising uranium decontaminated from plutonium and neptunium, the partition comprising:
b 1 ) a stripping of the plutonium present in the first organic phase, the plutonium being stripped in oxidation state III and the stripping comprising putting the first organic phase in contact with a third aqueous phase comprising nitric acid, a reducing agent which reduces plutonium(IV) to plutonium(III) and neptunium(VI) to neptunium(IV) without reducing uranium(VI), and an anti-nitrous agent, and then separating the first organic phase from the third aqueous phase;
b 2 ) a washing of the first organic phase from b 1 ) to remove from the first organic phase the plutonium fraction not having been stripped during b 1 ), the washing comprising putting the first organic phase in contact with a fourth aqueous phase comprising nitric acid, a reducing agent and an anti-nitrous agent identical to the reducing agent and the anti-nitrous agent used in b 1 ), and then separating the first organic phase from the fourth aqueous phase;
b 3 ) a washing of the third aqueous phase from b 1 ) to remove from the third aqueous phase the fraction of uranium(VI) and of neptunium(IV) having been stripped during b 1 ), the washing comprising putting the third aqueous phase in contact with a second organic phase comprising tri-n-butyl phosphate in an organic diluent, and then separating the second organic phase from the third aqueous phase;
b 4 ) a decontamination of uranium(VI) from neptunium(IV), the decontamination comprising a stripping of the neptunium(IV) present in the first organic phase from b 2 ), by putting the first organic phase in contact with a fifth aqueous phase comprising nitric acid and the diglycolamide, and then separating the first organic phase from the fifth aqueous phase, and a washing of the fifth aqueous phase stemming from the neptunium(IV) stripping, by putting the fifth aqueous phase in contact with a third organic phase comprising tri-n-butyl phosphate in an organic diluent, and then separating the third organic phase from the fifth aqueous phase; and
b 5 ) a stripping of the uranium(VI) present in the first organic phase from b 4 ), the stripping comprising putting the first organic phase in contact with a sixth aqueous phase comprising nitric acid, and then separating the first organic phase from the sixth aqueous phase.

11. The method of claim 9 , comprising:
a) a treatment of a first aqueous phase resulting from a dissolution of a spent nuclear fuel in nitric acid and comprising uranium(IV), plutonium(IV), neptunium(VI), actinides(III) and fission products, to decontaminate uranium(VI), plutonium(IV) and neptunium(VI) from the actinides(III) and fission products, the treatment comprising:
a 1 ) a co-extraction of uranium(VI), plutonium(IV) and neptunium(VI) from the first aqueous phase, the co-extraction comprising putting the first aqueous phase in contact with an organic phase comprising tri-n-butyl phosphate in an organic diluent, and then separating the organic phase from the first aqueous phase; and
a 2 ) a washing of the organic phase from a 1 ), the washing comprising putting the organic phase into contact with a second aqueous phase comprising nitric acid, and then separating the organic phase from the second aqueous phase;

whereby a first organic phase is obtained, which comprises uranium(VI), plutonium(IV) and neptunium(VI);
b) a partition of the uranium and the plutonium present in the first organic phase into two aqueous solutions, a first aqueous solution comprising plutonium and uranium decontaminated from neptunium and a second aqueous solution comprising uranium decontaminated from neptunium and plutonium, the partition comprising:
b 1 ) a stripping of the plutonium and of a fraction of the uranium present in the first organic phase, the plutonium being stripped in oxidation state III and the stripping comprising putting the first organic phase in contact with a third aqueous phase comprising nitric acid, a reducing agent which reduces plutonium(IV) to plutonium(III) and neptunium(VI) to neptunium(IV) without reducing uranium(VI), and an anti-nitrous agent, and then separating the first organic phase from the third aqueous phase;
b 2 ) a washing of the first organic phase from b 1 ) to remove from the first organic phase the plutonium fraction not having been stripped during b 1 ), the washing comprising putting the first organic phase in contact with a fourth aqueous phase comprising nitric acid, a reducing agent and an anti-nitrous agent identical to the reducing agent and the anti-nitrous a

Assignees

• Commissariat Energie Atomique
• Orano Cycle

Inventors

• Bernier Gilles
• Sorel Christian
• Miguirditchian Manuel
• Balaguer Coralie
• Ameil Estelle

Classifications

• G21F9/30

  Processing (separating different isotopes of the same chemical element B01D59/00) · CPC title

• G21F9/06

  Processing (separating different isotopes of the same chemical element B01D59/00) · CPC title

• G21C19/46 Primary

  Aqueous processes {, e.g. by using organic extraction means, including the regeneration of these means} · CPC title

• G21C19/44 Primary

  of irradiated solid fuel · CPC title

• C22B60/04

  Obtaining plutonium · CPC title