Method for conditioning ion exchange resins and apparatus for carrying out the method

Patent metadata

Field	Value
Publication number	US-12033766-B2
Application number	US-201917413365-A
Country	US
Kind code	B2
Filing date	Nov 28, 2019
Priority date	Dec 12, 2018
Publication date	Jul 9, 2024
Grant date	Jul 9, 2024

Abstract

A method for conditioning of spent ion exchange resins from nuclear facilities comprises the steps of: mixing the spent ion exchange resins with water to form a reaction mixture; setting and controlling the pH of the reaction mixture in a range from 1.0 to 3.5, preferably in a range from 2.0 to 3.0; adding an oxidant to the reaction mixture, with the temperature of the reaction mixture maintained at 90°° C. or less so that the spent ion exchange resin and the oxidant react with each other to form an aqueous reaction solution comprising the organic reaction products of the spent ion exchange resin; and electrochemically oxidizing the organic reaction products, wherein carbon dioxide is produced and a carbon-depleted aqueous reaction solution having a TOC (total organic carbon) value of less than 50 ppm is obtained. Furthermore, an apparatus for the conditioning of spent ion exchange resins from nuclear facilities is described.

First claim

The invention claimed is:

1. A method for conditioning of spent ion exchange resins from nuclear facilities, comprising the steps of:
mixing the spent ion exchange resins with water to form a reaction mixture;
setting and monitoring the pH of the reaction mixture in a range from 1.0 to 3.5;
adding an oxidant to the reaction mixture, with the temperature of the reaction mixture maintained at 90° C. or less, so that the spent ion exchange resin and the oxidant react with each other to form an aqueous reaction solution comprising organic reaction products of the spent ion exchange resin; and
electrochemically oxidizing the organic reaction products in the reaction solution by means of a boron-doped diamond electrode, wherein carbon dioxide is produced and a carbon-depleted aqueous reaction solution having a TOC (total organic carbon) value of less than 50 ppm is obtained.

2. The method according to claim 1 , characterized in that the ion exchange resins contain organic complexing agents.

3. The method according to claim 1 , characterized in that the reaction mixture comprises water and spent ion exchange resin in a volume ratio of 3:1 to 1.5:1.

4. The method according to claim 1 , characterized in that the temperature of the reaction mixture is maintained in a range from 60 to 90° C.

5. The method according to claim 1 , characterized in that the pH of the reaction mixture is set and controlled by the addition of a mineral acid or a base.

6. The method according to claim 1 , characterized in that the oxidant is an aqueous solution of hydrogen peroxide at a concentration of 30 to 35 weight percent.

7. The method according to claim 1 , characterized in that the hydrogen peroxide is added to the reaction mixture such that the concentration of hydrogen peroxide in the reaction mixture is at least 20,000 ppm.

8. The method according to claim 1 , characterized in that no antifoaming agent is added to the reaction mixture.

9. The method according to claim 1 , characterized in that the addition of the oxidant is terminated and the electrochemical oxidation is started when the aqueous reaction solution becomes a clear and transparent solution.

10. The method according to claim 1 , characterized in that the electrochemical oxidation is performed at a voltage of 5 V or less.

11. The method according to claim 1 , characterized in that, prior to the electrochemical oxidation, water from the reaction mixture and/or the aqueous reaction solution is removed from the reaction vessel by means of vacuum distillation.

12. The method according to claim 11 , characterized in that the water removed by vacuum distillation is purified by means of reverse osmosis to contain volatile organic substances, and the volatile organic substances are returned to the reaction mixture and/or the aqueous reaction solution.

13. The method of claim 1 , wherein the range of the reaction mixture pH is 2.0 to 3.0.

14. The method of claim 1 , wherein the oxidant is an aqueous solution of hydrogen peroxide.

15. The method of claim 1 , wherein the reaction mixture is maintained at 85° C. or less.

16. The method of claim 3 wherein the volume ratio of the water and spent ion exchange resin is 2.5:1 to 2:1.

17. The method of claim 4 wherein the temperature range of the reaction mixture is 70 to 85° C.

18. The method of claim 5 wherein the mineral acid is sulfuric acid or nitric acid.

19. The method of claim 5 wherein the base is alkali hydroxide or alkaline earth hydroxide.

20. An apparatus for conditioning of spent ion exchange resins, comprising:
a reaction vessel for the accommodation of the spent ion exchange resins and water;
an oxidant supply that is connected to the reaction vessel;
a vacuum distillation unit comprising a spray column that is connected to the reaction vessel and a condenser; and
a unit for electrochemical oxidation that is arranged within the reaction vessel or connected to it, with the unit for electrochemical oxidation having a boron-doped diamond electrode.

21. The facility according to claim 20 , characterized in that the condenser is connected to a reverse osmosis unit.

22. The facility according to claim 20 , characterized in that the unit for electrochemical oxidation comprises a reactor and a boron-doped diamond electrode, wherein the reactor is connected to the reaction vessel and the boron-doped diamond electrode is arranged in the reactor.

Assignees

• Framatome Gmbh

Inventors

• Seybert Gert
• Lehr Robert
• Zeiler Bertram
• Schuberth Philip
• Weiss Steffen

Classifications

• G21F9/30

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

• B01J2219/0879

  Solid · CPC title

• B01J45/00

  Ion-exchange in which a complex or a chelate is formed; Use of material as complex or chelate forming ion-exchangers; Treatment of material for improving the complex or chelate forming ion-exchange properties (ion-exchange chromatography processes B01D15/36) · CPC title

• B01J49/30

  Electrical regeneration · CPC title

• B01J49/50

  characterised by the regeneration reagents · CPC title