US2004045935A1PendingUtilityA1
Method for dissolving solids formed in a nuclear installation
Priority: Dec 4, 2000Filed: Dec 4, 2001Published: Mar 11, 2004
Est. expiryDec 4, 2020(expired)· nominal 20-yr term from priority
Inventors:Alastair Magnaldo
C23G 1/14G21F 9/004C23G 1/02
36
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Claims
Abstract
Method of dissolving the solids formed in the apparatus and pipework of a nuclear plant, in which said solids are brought into contact with an aqueous dissolving solution chosen from aqueous solutions of carbonate ions having a concentration of greater than or equal to 0.3M, aqueous solutions of bicarbonate ions, and solutions of a mixture of nitric acid and of a polycarboxylic acid chosen from oxalic acid and triacids.
Claims
exact text as granted — not AI-modified1 . Method of dissolving the solids formed in the apparatus and pipework of a nuclear plant, in which said solids are brought into contact with an aqueous dissolving solution chosen from aqueous solutions of carbonate ions having a concentration of greater than or equal to 0.3M, aqueous solutions of bicarbonate ions, and solutions of a mixture of nitric acid and of a polycarboxylic acid chosen from oxalic acid and triacids.
2 . Method according to claim 1 , in which the contacting is carried out at a temperature of 20° C. to 80° C. for a time of 1 to 24 hours.
3 . Method according to claim 1 , in which the aqueous dissolving solution is a carbonate ion solution.
4 . Method according to claim 3 , in which the carbonate ion concentration of the aqueous dissolving solution is from 0.3M to the solubility limit in water of the carbonate salt from which the ion derives.
5 . Method according to either of claims 3 and 4 , in which the carbonate ions derive from a salt chosen from carbonates of alkali metals such as sodium and potassium, carbonates of alkaline-earth metals and ammonium carbonates.
6 . Method according to any one of claims 3 to 5 , in which, after the contacting step, an acid solution, preferably a nitric acid solution, is added to the aqueous dissolving solution.
7 . Method according to any one of claims 3 to 6 , in which the volume of dissolving solution is from 3 ml to 100 ml per g of solids.
8 . Method according to claim 1 , in which the aqueous dissolving solution is a bicarbonate ion solution with a concentration of 0 to 2M.
9 . Method according to claim 1 , in which the aqueous dissolving solution is an aqueous solution comprising a mixture of nitric acid and of a polycarboxylic acid chosen from oxalic acid and triacids.
10 . Method according to claim 9 , in which the nitric acid concentration is from 0.05 to 1M and the polycarboxylic acid concentration is from 0.3M to 1M.
11 . Method according to either of claims 9 and 10 , in which the polycarboxylic acid is citric acid.
12 . Method according to any one of claims 9 to 11 , in which, after the contacting step, the acids of the dissolving solution are destroyed by oxidation.
13 . Method according to any one of claims 1 to 12 , in which the compound or compounds involved in the composition of the solids to be dissolved is/are chosen from:
zirconium molybdate and mixed zirconium plutonium molybdate;
zirconium phosphates and associated gels;
cesium phosphomolybdate;
plutonium phosphate;
molybdenum, zirconium and plutonium oxides;
iron phosphate; and
barium sulphate.Join the waitlist — get patent alerts
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