GB2105096A - Process for the reprocessing of irradiated nuclear fuels - Google Patents

Process for the reprocessing of irradiated nuclear fuels Download PDF

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Publication number
GB2105096A
GB2105096A GB08216895A GB8216895A GB2105096A GB 2105096 A GB2105096 A GB 2105096A GB 08216895 A GB08216895 A GB 08216895A GB 8216895 A GB8216895 A GB 8216895A GB 2105096 A GB2105096 A GB 2105096A
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GB
United Kingdom
Prior art keywords
residue
reprocessing
plutonium
fuels
irradiated nuclear
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
GB08216895A
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GB2105096B (en
Inventor
Roger De Meester
Lothar Koch
Michel Coquerelle
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European Atomic Energy Community Euratom
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European Atomic Energy Community Euratom
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Publication of GB2105096A publication Critical patent/GB2105096A/en
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Publication of GB2105096B publication Critical patent/GB2105096B/en
Expired legal-status Critical Current

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    • GPHYSICS
    • G21NUCLEAR PHYSICS; NUCLEAR ENGINEERING
    • G21CNUCLEAR REACTORS
    • G21C19/00Arrangements for treating, for handling, or for facilitating the handling of, fuel or other materials which are used within the reactor, e.g. within its pressure vessel
    • G21C19/42Reprocessing of irradiated fuel
    • G21C19/44Reprocessing of irradiated fuel of irradiated solid fuel
    • G21C19/48Non-aqueous processes
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E30/00Energy generation of nuclear origin
    • Y02E30/30Nuclear fission reactors
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02WCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
    • Y02W30/00Technologies for solid waste management
    • Y02W30/50Reuse, recycling or recovery technologies

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  • Physics & Mathematics (AREA)
  • Engineering & Computer Science (AREA)
  • Plasma & Fusion (AREA)
  • General Engineering & Computer Science (AREA)
  • High Energy & Nuclear Physics (AREA)
  • Inorganic Compounds Of Heavy Metals (AREA)
  • Processing Of Solid Wastes (AREA)

Abstract

In the reprocessing of irradiated nuclear fuels, wherein a radioactive residue occurs which is insoluble in acid, this residue, after drying, is rendered soluble by being treated at a relatively high temperature with a dry alkali hydroxide under oxidizing conditions.

Description

SPECIFICATION Process for the reprocessing of irradiated nuclear fuels The present invention relates to the reprocessing of irradiated nuclear fuels.
During the reprocessing of fuels containing plutonium, in accordance with the known PUREX process, insoluble residues are obtained which, interalia, contain plutonium. According to the production conditions of the fuel and the irradiation conditions, this residue can amount to as much as several percent of the plutonium used.
The residue is highly radioactive and very dangerous, and it is absolutely necessary for it to be brought into a soluble state and processed further.
The present invention lies in treating the dry residue, which is not soluble in nitric acid or other strong acids and which arises in the first stage of the PUREX process, with dry alkali hydroxides under oxidizing conditions and at a high temperature.
Preferably, the dry residue is heated in a molar ratio of about 1:4 very intimately mixed with NaOH and is dried at 1 200C in dry air free of CO2, or in an equivalent oxidizing gas stream, for about 12 hours between 550 and 800 C.
Accordingly, interalia the Pu contained in the residue, which is insoluble in nitric acid, is converted into its ternary oxide having the empirical formula NaePuOs. Under the reaction conditions, soluble ternary oxides of the fission products are also partly formed. The conversion to the corresponding americium compound is incomplete, since at these temperatures the high-valency ternary americium oxides are no longer stable.
A number of experiments were carried out in accordance with the above-described process. At least 99% of the 270 mg of PuO2 present in a residue of 1100 mg were dissolved. (Since undissolved AmO2 was still present, 3 mg was the detection limit for Pu.) In the case of an assumed residue of PuO2 of 2%, a decomposition of 99% of the residue signifies that 99.98% of the plutonium can be fed to the recovery process.
It should be mentioned that the reaction product could be dissolved in 3 to 6 molar HNO3 (according to the requirements of the PUREX-Feed-solution).
The additional feed of NaN03 into the process will lie within the order of magnitude of the NaNO3 present.
As already mentioned, in the process according to the invention the plutonium losses are reduced during reprocessing. Not only the economy of the Pu cycle is improved, but also the toxicity of the waste is reduced. It is possible to avoid the expensive production processes which lead to a multiplication of the production cost of plutonium-containing fuels.
Example 1100 mg of residue with 270 mg of PuO2 and 7 mg of AmO2 were heated with NaOH for 12 hours at 600"C in a silver vessel, in accordance with the invention. The resultant product was dissolved in nitric acid and filtered. In the filter residue Pu and Am were no longer measurable.
1. A process for the reprocessing of irradiated nuclear fuels, wherein a residue occurs which is insoluble in acid, characterised in that the residue, after drying, is treated at a relatively high temperature with an alkali hydroxide under oxidizing conditions.
2. A process as claimed in claim 1, wherein the residue is heated for about 12 hours at from 550 to 800"C with NaOH.
3. A process as claimed in claim 1 substantially as hereinbefore described.
4. A process as claimed in claim 1 substantially as hereinbefore described in the specific Example.
**WARNING** end of DESC field may overlap start of CLMS **.

Claims (4)

**WARNING** start of CLMS field may overlap end of DESC **. SPECIFICATION Process for the reprocessing of irradiated nuclear fuels The present invention relates to the reprocessing of irradiated nuclear fuels. During the reprocessing of fuels containing plutonium, in accordance with the known PUREX process, insoluble residues are obtained which, interalia, contain plutonium. According to the production conditions of the fuel and the irradiation conditions, this residue can amount to as much as several percent of the plutonium used. The residue is highly radioactive and very dangerous, and it is absolutely necessary for it to be brought into a soluble state and processed further. The present invention lies in treating the dry residue, which is not soluble in nitric acid or other strong acids and which arises in the first stage of the PUREX process, with dry alkali hydroxides under oxidizing conditions and at a high temperature. Preferably, the dry residue is heated in a molar ratio of about 1:4 very intimately mixed with NaOH and is dried at 1 200C in dry air free of CO2, or in an equivalent oxidizing gas stream, for about 12 hours between 550 and 800 C. Accordingly, interalia the Pu contained in the residue, which is insoluble in nitric acid, is converted into its ternary oxide having the empirical formula NaePuOs. Under the reaction conditions, soluble ternary oxides of the fission products are also partly formed. The conversion to the corresponding americium compound is incomplete, since at these temperatures the high-valency ternary americium oxides are no longer stable. A number of experiments were carried out in accordance with the above-described process. At least 99% of the 270 mg of PuO2 present in a residue of 1100 mg were dissolved. (Since undissolved AmO2 was still present, 3 mg was the detection limit for Pu.) In the case of an assumed residue of PuO2 of 2%, a decomposition of 99% of the residue signifies that 99.98% of the plutonium can be fed to the recovery process. It should be mentioned that the reaction product could be dissolved in 3 to 6 molar HNO3 (according to the requirements of the PUREX-Feed-solution). The additional feed of NaN03 into the process will lie within the order of magnitude of the NaNO3 present. As already mentioned, in the process according to the invention the plutonium losses are reduced during reprocessing. Not only the economy of the Pu cycle is improved, but also the toxicity of the waste is reduced. It is possible to avoid the expensive production processes which lead to a multiplication of the production cost of plutonium-containing fuels. Example 1100 mg of residue with 270 mg of PuO2 and 7 mg of AmO2 were heated with NaOH for 12 hours at 600"C in a silver vessel, in accordance with the invention. The resultant product was dissolved in nitric acid and filtered. In the filter residue Pu and Am were no longer measurable. CLAIMS
1. A process for the reprocessing of irradiated nuclear fuels, wherein a residue occurs which is insoluble in acid, characterised in that the residue, after drying, is treated at a relatively high temperature with an alkali hydroxide under oxidizing conditions.
2. A process as claimed in claim 1, wherein the residue is heated for about 12 hours at from 550 to 800"C with NaOH.
3. A process as claimed in claim 1 substantially as hereinbefore described.
4. A process as claimed in claim 1 substantially as hereinbefore described in the specific Example.
GB8216895A 1981-06-24 1982-06-10 Process for the reprocessing of irradiated nuclear fuels Expired GB2105096B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
LU83452A LU83452A1 (en) 1981-06-24 1981-06-24 METHOD FOR REPROCESSING IRRADIATED NUCLEAR FUELS

Publications (2)

Publication Number Publication Date
GB2105096A true GB2105096A (en) 1983-03-16
GB2105096B GB2105096B (en) 1985-10-09

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Family Applications (1)

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GB8216895A Expired GB2105096B (en) 1981-06-24 1982-06-10 Process for the reprocessing of irradiated nuclear fuels

Country Status (6)

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BE (1) BE893514A (en)
DE (1) DE3221688A1 (en)
FR (1) FR2508692B1 (en)
GB (1) GB2105096B (en)
IT (1) IT1148342B (en)
LU (1) LU83452A1 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102010036737A1 (en) * 2010-07-29 2012-02-02 Erwin Krüger Process for the dry reprocessing of spent nuclear fuel (irradiated) and an apparatus for carrying out the process

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1199748B (en) * 1963-05-15 1965-09-02 Kernforschung Mit Beschraenkte Process for processing irradiated nuclear fuel
DE1467322B2 (en) * 1964-06-10 1972-06-22 Europäische Atomgemeinschaft (EURATOM), Brüssel PROCESS FOR THE RECYCLING OF OXYDIC NUCLEAR REACTOR FUEL
FR1483117A (en) * 1965-06-10 1967-06-02 Kernforschungsanlage Juelich Process for the preparation of coated nuclear fuels

Also Published As

Publication number Publication date
GB2105096B (en) 1985-10-09
LU83452A1 (en) 1981-10-29
FR2508692A1 (en) 1982-12-31
IT8248692A0 (en) 1982-06-23
IT1148342B (en) 1986-12-03
FR2508692B1 (en) 1988-08-05
BE893514A (en) 1982-10-01
DE3221688A1 (en) 1983-01-13

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