JPS5528373A - Uranium sampling method - Google Patents
Uranium sampling methodInfo
- Publication number
- JPS5528373A JPS5528373A JP10187978A JP10187978A JPS5528373A JP S5528373 A JPS5528373 A JP S5528373A JP 10187978 A JP10187978 A JP 10187978A JP 10187978 A JP10187978 A JP 10187978A JP S5528373 A JPS5528373 A JP S5528373A
- Authority
- JP
- Japan
- Prior art keywords
- chelate
- metal ions
- dissolved
- ion exchange
- adsorbed
- 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.)
- Pending
Links
Landscapes
- Treatment Of Water By Ion Exchange (AREA)
- Manufacture And Refinement Of Metals (AREA)
Abstract
PURPOSE: To sample U especially from the sea water, by contacting the U dissolved solution with chelate ion exchange resin having metal ions absorbed to absorb dissolved U, and then contacting with NH4Cl, (NH4)2CO3, or the like.
CONSTITUTION: Chelate ion exchange resin having metal ions such as Ti and iron adsorbed is contacted with U dissolved solution of low concetration such as sea water and waste water from nuclear reactor, and dissolved U is adsorbed. In this adsorption process, it is preferable to keep the value of pH of U dissolved solution at 4 to 8, especially under weak acidic state, and the adsorption capacity is further increased when the water temperature is kept above 50°C. Then, the chelate resin with metal ions having U adsorbed is contacted with aqueous solution of more than one kind of salts selected from NH4Cl, Na2CO3 and (NH4)2CO3 to desorb U. The concentration of salt at this time should be preferably 0.5 to 2 mols, and it is advantageous to perform desorption operation at higher than pH 4. As for metal ions, it is preferable to use Ti ions. As for the chelate resin, chelate ion exchange resin of which chelate forming functional group is polyamine is used.
COPYRIGHT: (C)1980,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10187978A JPS5528373A (en) | 1978-08-23 | 1978-08-23 | Uranium sampling method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10187978A JPS5528373A (en) | 1978-08-23 | 1978-08-23 | Uranium sampling method |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS5528373A true JPS5528373A (en) | 1980-02-28 |
Family
ID=14312227
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP10187978A Pending JPS5528373A (en) | 1978-08-23 | 1978-08-23 | Uranium sampling method |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5528373A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS57123939A (en) * | 1980-12-15 | 1982-08-02 | Kernforschungsanlage Juelich | Method of enrichening uranium from sea water |
-
1978
- 1978-08-23 JP JP10187978A patent/JPS5528373A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS57123939A (en) * | 1980-12-15 | 1982-08-02 | Kernforschungsanlage Juelich | Method of enrichening uranium from sea water |
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