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ORNL-1771 - Oak Ridge National Laboratory

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uranium hexafluoride with a molten NaF-ZrF, salt<br />

bath (at 65OOC) in which the UF, is insoluble in<br />

the presence of excess fluorine. The uraniurn loss<br />

in the scrubbing step was less than 0.001%. Frac-<br />

tional distillation of the UF, from this step, which<br />

would be performed in order to obtain complete<br />

decontamination, could be carried out in only lightly<br />

shielded equipment.<br />

Two experiments on scrubbing UF, with molten<br />

NaF-ZrF, were carried out. In one, un acetone-dry<br />

ice cold trap was used between the fluorination and<br />

scrub steps; the uranium hexafluoride was con-<br />

densed (and thus separated from excess fluorine)<br />

in the cold trap and was then resublimed from it.<br />

The uranium was recovered from the scrub salt by<br />

Gross<br />

Ru<br />

Zr<br />

ldb<br />

TRE<br />

cs<br />

Sr<br />

Ba<br />

PERIOD ENDING SEPTEMBER 70, 1954<br />

refluorination. In the second experiment no cold<br />

trap wos used, but the decontamination obtained<br />

was the same (Table 1.1). It is thought that<br />

resublimation of the salt-scrubbed product would<br />

achieve additional decontamination.<br />

Synethetic ARE fuel was prepared for the two<br />

runs by dissosving a 224-day-irrodiated, 30-day-<br />

cooled, 6-9 miniature uranium slug in NaF-ZrF,<br />

(56-44 mole %) at 650°C by passing HF through<br />

the molten bath. The final NaF-ZrF,-UF, mixture<br />

had a composition of 54.0-42.4-3.6 mole % and<br />

activity of 5 x lo6 beta counts per minute per<br />

milligram of uranium. The dissolution and subse-<br />

quent fluorination were carried aut in the same<br />

nickel reactor. in each run the scrub salt was<br />

TABLE 1-11. DECONTAMlNATlON OBTAINED BY MOLTEN SALT SCRUBBING OF UF6<br />

IN THE FLUORIDE VOLATlLlT'Y PROCESS<br />

6<br />

Synthetic ARE fuel; beta activity of 5 x 10 counts per minute per milli-<br />

Act; vi ty<br />

gram of uranium; fluorinated at 650°C with elemental fluorine gas at flow<br />

rate of 66 rnl/rnin<br />

Run A:<br />

Run B:<br />

In fluorination salt<br />

In resublimation trap<br />

In scrub salt<br />

Fluorination period of 3 hr; UF plus excess fluorine passed<br />

6<br />

directly<br />

to scrub salt from the fluorination step<br />

Fluorination period of 5hr; UFg condensed in cold trap andrcsub-<br />

limed from it prior to scrubbing and recovered from scrub by re-<br />

fluorination<br />

Run A<br />

Beta Decontamination Factors<br />

.......................................... ___<br />

Run B<br />

. ............................ ~<br />

Scrub Over-al I Scrub Oves-all<br />

2 x 10,"<br />

2 x IO4*<br />

6 750 1.4 430<br />

3 >7 x IO4<br />

9 1 x IO5<br />

4 700 8<br />

4<br />

a Y 10<br />

90 >8 x 104 3 2 x IO4<br />

4<br />

130 '~3 x 16<br />

20 23 ,? 106<br />

>8 ? IO5<br />

Uranium Losses (X of Initial Charge)<br />

l*4<br />

0.23<br />

131<br />

*Calculated onthe gross Ru, Zr, bib, and 'TRE activity rather khan on *otd activity, which included much due to I .<br />

This does not materially affect comparison with pruwioi~s gross beta decontcmination datu,<br />

3 x<br />

0.74<br />

40-3<br />

13

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