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- Author or Editor: J. Kadrabová x
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Abstract
The extraction of the pertechnetate anion has been investigated in the systems tributylphosphate (TBP)—solvent (carbon tetrachloride, n-heptane, chloroform)—metal salt (uranyl nitrate and chloride, thorium nitrate)—ammonium salt. In the absence of a metal, the solvates HTeO4. iTBP (i=4) are extracted, while in the presence of uranium and thorium, the distribution of technetium corresponds to the formation of the mixed complexes: UO2(NO3)(TeO4)·2TBP, UO2Cl(TcO4)·2TBP and Th(NO3)3 (TcO1)·2TBP. The effective constants of the reactions H++TcO 4 − +i(TBP)org←(HTcO1·iTBP)org, and (MLn·2TBP)org+TcO 4 − ←(MLn−1TcO4·2TBP)org+L were established in the above systems. The extraction of pertechnetate ion is more effective when it is coordinated to a cation solvated by TBP than the extraction in the form of pertechnetate acid solvated by TBP.
Abstract
The extraction of reduced99mTc with 5,7-dichloroxine, tributyl phosphate (TBP) and 1-phenyl-3-methyl-4-benzoyl-pyrazolone-5 (PMBP) from HCl−LiCl mixtures has been studied. A mechanism of extraction is proposed and the stability of the chlorocomplexes of technetium (V) in a hydrochloric and—lithium chlorid—perchloric acid mixture has been established using extraction data of99mTc and spectrophotometric measurements with99Tc.
