EDTA and mixed-ligand complexes of tetravalent and trivalent plutonium

EDTA forms stable complexes with plutonium that are integral to nuclear material processing, radionuclide decontamination, and the potentially enhanced transport of environmental contamination. To characterize the aqueous Pu(4+/3+)EDTA species formed under the wide range of conditions of these processes, potentiometry, spectrophotometry, and cyclic voltammetry were used to measure solution equilibria. The results reveal new EDTA and mixed-ligand complexes and provide more accurate stability constants for previously identified species. In acidic solution (pH < 4) and at 1:1 ligand to metal ratio, PuY (where Y4- is the tetra-anion of EDTA) is the predominant species, with an overall formation constant of log beta(110) = 26.44. At higher pH, the hydrolysis species, PuY(OH)(-) and PuY(OH)(2)(2-), form with the corresponding overall stability constants log beta(11-1) = 21.95 and 109 beta(11-2) = 15.29, The redox potential of the complex PuY at pH = 2.3 was determined to be E-1/2 = 342 mV. The correlation between redox potential, pH, and the protonation state of PuY- was derived to estimate the redox potential of the pU(4+/3+)y complex as a function of pH. Under conditions of neutral pH and excess EDTA relative to Pu4+, PuY24- forms with an overall formation constant of log beta(120) = 35.39. In the presence of ancillary ligands, mixed-ligand complexes form, as exemplified by the citrate and carbonate complexes PuY(citrate)(3-) (log beta(1101) = 33.45) and PuY(carbonate)(2)(log beta(1101) = 35.51). Cyclic voltarnmetry shows irreversible electrochemical behavior for these coordinatively saturated Pu4+ complexes: The reduction wave is shifted approximately -400 mV from the reduction wave of the complex PuY, while the oxidation wave is invariant.