THE RADIOCHEMISTRY OF PLUTONIUM - Sciencemadness.org
THE RADIOCHEMISTRY OF PLUTONIUM - Sciencemadness.org
THE RADIOCHEMISTRY OF PLUTONIUM - Sciencemadness.org
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95% of Pu(IV) was removed from a 0.5 ~ Na2C03 solution by passage of 2000-bed<br />
volumes at a flow rate of 1 ml/ cm2/min of the solution through an HTO column. The<br />
absorption of Pu(IV) was not affected by tb.e pre aence of 5 mg/ 1 of U (VI). The absorp-<br />
tion of Pu(VI) was only 20~0 in 1000-bed volumes under the same conditions. A possible<br />
application of this system to recover Pu and other ions from carbonate wastes in<br />
processing plants is discussed.<br />
Paper Chromatography<br />
Clanet 90 determined paper chromatographic Rf values for Pu(III), Pu(IV)<br />
and Pu(VI), U(IV)J and U(VI), and Am(lII) in HC1-butanol mixtures (1:1) ranging from<br />
1 to 10 M HC1. The Rf values “reached a matium around 6 M HC1 and ranged from<br />
— —<br />
0.27 for U(m) to 0.50 for U(VI), the other ions falling in between. The ions of lower<br />
valency tended to have lower Rf values.<br />
47<br />
Bildestein et al. separated U and Pu by several paper cbromatographic<br />
methods, using different combinations of solvent and acid. The use of ion-exchange<br />
paper to separate U and Pu was also reported by these w“orkers. For example, with<br />
Whatman ET-20 using 6 M HC1 as a developer, the Rf values are 0.56 and 0.98 for U<br />
—<br />
and Pu, respectively. The oxidation states of the U and Pu were not specified.<br />
Fink and Fink ’31 mve stigated many combinations of solvent and acid to<br />
develop paper chromatograms of both Pu(IV) and Pu(VI). In most systems PuOV)<br />
failed to move or streaked, but in a few cases moved quantitatively. The results<br />
indicated Pu(VI) and U(VI) might be separated in a methyl ethyl ketone - dilute nitric<br />
acid system.<br />
Anion Exchange<br />
The behavior of the actinide elements in various oxidation states on a<br />
strong base anion exchange resin (typically Dowex 1 or 2) in HC1. is shown in Table IV-<br />
29. Strong adsorption of the actinides in the higher ondation states (IV-VI) occurs at<br />
HC1 concentrations above 6 ~ while resorption occurs below 2 M HC1.<br />
—<br />
TABLE IV- 29. Absorption and Resorption of Actinides on Strong Base Anion<br />
Exchangers in HC1 Solutions<br />
Oxidation State of<br />
HC1 Concentration(~) for<br />
Actinide Absorption(a) Resorption@)<br />
m Not absorbed<br />
IV 6-8 2-4<br />
v 6-8 2-4<br />
VI 2-3 0.1-1<br />
(a)Kd . lo-10o for absorption.<br />
(b) Kd = 0.1-1.0 for resorption.<br />
A convenient way of separating Pu from other actinides and most other<br />
elements is to adsorb Pu(IV) or Pu(VI) onto such a resin from > 6 M HC1 solution,<br />
—<br />
wash with HC1, and desorb by reducing the Pu to the trivalent with a suitable reducing<br />
84