The Decontamination of Uranium from Fission Products by the Use of the Uranyl Oxalate Precipitation Reaction Page: 5
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few;-
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/life •: >feir'inwv:;:
lilt
•ms*
CQ>JFID®mAl-
tlon*type reactions.
The urmniua pere&tde reaction (30* 8«0» M precipitant) and tha
urmnyl onalabs reaction (fl*C*<vai#0 u precipitant) art both used
extend vs ly mi thle laboratory for rifuUr cbeeical purlf teat loo.
Tbit nport dsacribes their uet Tor the separation of ureniua free
WM
flttloQ product*.
II - Experimental Consideration*
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1. nature of activity at th* tla* of attested decontamination,
It wee assumed at the outset of the problem that a cooling
period would bo allowed prior to attempted decontamination. This
would decrease the initial activity by perhaps half and leave coat
11 gs . - ^ ’
esdiua-llved, but chiefly long-lived, isotopes. This cooling period
m
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Kelchner, B. L. The Decontamination of Uranium from Fission Products by the Use of the Uranyl Oxalate Precipitation Reaction, report, May 10, 1951; [Oak Ridge, Tennessee]. (https://digital.library.unt.edu/ark:/67531/metadc502333/m1/4/: accessed April 16, 2024), University of North Texas Libraries, UNT Digital Library, https://digital.library.unt.edu; crediting UNT Libraries Government Documents Department.