Open AccessActinide(IV) and actinide(VI) carbonate speciation studies by PAS and NMR spectroscopies; Yucca Mountain Project: Milestone report 3031-WBS 1.2.3.4.1.3.1
Author(s) -
David L. Clark,
Solveig Ekberg,
D. E. Morris,
Phillip D. Palmer,
C. Drew Tait
Publication year - 1994
Language(s) - English
Resource type - Reports
DOI - 10.2172/145483
Subject(s) - carbonate , chemistry , actinide , carbonate ion , inorganic chemistry , nuclear magnetic resonance spectroscopy , ligand (biochemistry) , analytical chemistry (journal) , nuclear chemistry , radiochemistry , stereochemistry , organic chemistry , biochemistry , receptor
Pulsed-laser photoacoustic spectroscopy (PAS) and Fourier-transform nuclear magnetic resonance (NMR) spectroscopy were used to study speciation of actinide(IV) and actinide(VI) ions (Np, Pu, Am) in aqueous carbonate solutions vs pH, carbonate content, actinide content, temperature. PAS focused on Pu(IV) speciation. Stability fields on a pH (8.4 to 12.0) versus total carbonate content (0.003 to 1.0 M) plot for dilute Pu(IV) carbonate species ([Pu]{sub tot} = 1 mM) were mapped. Four plutonium species, with absorption peaks at 486, 492, 500, and 512 nm were found. Loss of a single carbonate ligand does not account for the difference in speciation for the 486 and 492 nm absorption peaks, nor can any of the observed species be identified as colloidal Pu(IV). NMR data have been obtained for UO{sub 2}{sup 2+}, PuO{sub 2}{sup 2+} and AmO{sub 2}{sup 2+}. This report focuses on results for PuO{sub 2}{sup 2+}. The ligand exchange reaction between free and coordinated carbonate on the PuO{sub 2}(CO{sub 3}){sub 3}{sup 4{minus}} systems has been examined by variable temperature {sup 13}C NMR spectroscopy. In each of the six different PuO{sub 2}(CO{sub 3}){sub 3}{sup 4{minus}} samples, two NMR signals are present, one for the free carbonate ligand and one for the carbonate ligand coordinated to a paramagnetic plutonium metal center. The single{sup 13}C resonance line for coordinated carbonate is consistent with expectations of a monomeric PuO{sub 2}(CO{sub 3}){sub 3}{sup 4{minus}} species in solution. A modified Carr-Purcell-Meiboom-Gill NMR pulse sequence was used for determining ligand exchange parameters for paramagnetic actinide complexes. Eyring analysis at standard conditions provided activation parameters of {Delta}H = 38 KJ/M and {Delta}S = {minus}60 J/K for the plutonyl triscarbonate system, suggesting an associative transition state for the plutonyl(VI) carbonate complex self-exchange reaction