GB1044085A - - Google Patents
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- Publication number
- GB1044085A GB1044085A GB1044085DA GB1044085A GB 1044085 A GB1044085 A GB 1044085A GB 1044085D A GB1044085D A GB 1044085DA GB 1044085 A GB1044085 A GB 1044085A
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- GB
- United Kingdom
- Prior art keywords
- acid
- organic
- aqueous phase
- aqueous
- americium
- 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.)
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- Manufacture And Refinement Of Metals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
1,044,085. Separation of americium and curium. UNITED STATES ATOMIC ENERGY COMMISSION. Aug. 4, 1964 [Sept. 18, 1963], No. 31260/64. Heading G6R. Americium (Am) or curium (Cm) is separated from yttrium or lanthanide rare earth fission products in an aqueous mixture by adding an aminopolycarboxylic acid or a salt thereof and a water-soluble organic acid, and then contacting the aqueous solution with an organic solution containing a monoacidic organophosphorus compound of the formula where R2 is alkyl and R3 is is alkyl or aryl. The organic phase containing fission products is separated from the aqueous phase containing Am or Cm. A number of suitable aminopolycarboxylic acids, organic acids, and organophosphorus compounds are listed; the diluent for the organophosphorus compound may be an aromatic hydrocarbon. The aqueous phase preferably has a pH of 1À5 to 4À0. The Am or Cm is removed from the aqueous phase by a second extraction with an organic solution in which the organophosphorus compound is different or is present in higher concentration, or in which an aliphatio hydrocarbon is used as diluent, the Am or Cm being returned to aqueous solution by extraction with HNO3 or HCl; alternatively oxalic acid is added to the aqueous phase to precipitate Am and Cm as oxalates. In Example I a solution containing americium,. cerium and europium is treated with lactic acid and the sodium salt of diethylenetriamiriepentaacetic acid, and extracted with di-(2-ethylhexyl) phosphoric acid in diisopropylbenzene. In other examples, components of the organic phase are decyl hydrogen decylphosphonate, diethylbenzene, and dodecane, and the organic acid is tartaric, citric, glycolic, or malonic acid.
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1044085A true GB1044085A (en) |
Family
ID=1755248
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB1044085D Active GB1044085A (en) |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB1044085A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2118759A (en) * | 1982-03-15 | 1983-11-02 | Euratom | Process for the recovery of plutonium from aqueous nitric solutions |
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0
- GB GB1044085D patent/GB1044085A/en active Active
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2118759A (en) * | 1982-03-15 | 1983-11-02 | Euratom | Process for the recovery of plutonium from aqueous nitric solutions |
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